{"title":"KEIFEI","description":null,"products":[{"product_id":"keifei-test-c-250","title":"Keifei Test C 250","description":"\u003cp\u003e\u003cspan\u003eKEIFEI T CYPBOLIN 250(250MG\/ML TESTOSTERONE CYPIONATE=10ML)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 15-16 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic Steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-1000mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes, common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes, due to water\/electrolyte retention\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low, except in absurd dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes, severely\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePretty much all that was written about TESTOSTERONE ENANTHATE also applies to TESTOSTERONE CYPIONATE. A slight distinction was made in that they\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eeach provided a notable different half- and active-life period. For this reason, CYPIONATE injections were reduced to every 8th day by some reported users. Dosages of 200-1000mg weekly were common, but most users experienced excellent results with 200-600mg weekly. Both testosterone preparations stacked well with any other AAS and added a distinct androgenic effect. This meant improved regenerative qualities and greater training intensity with a correlating significant increase in weight-load capacity. For those who wished to use testosterone but were highly sensitive to gyno and water\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eretention, TESTOSTERONE PROPIONATE was commonly reported to be the better\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003echoice. Oddly enough, a few of those polled reported more sensitively due to Propionate’s fast action. Interesting paradox, huh? The issue was simply a matter of dosage\/administration protocols. Since PROPIONATE remained active for about 3 days a weekly administration protocol allowed circulatory clearing of the drug. It should be\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003enoted that both TESTOSTERONE ENANTHATE and CYPIONATE were said to be\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003emore anabolic and less androgenic then SUSPENSION or PROPIONATE. This is pure imagination. The truth is that suspension actually is a faster acting testosterone and contains more total testosterone per 100mg dosage than any esterfied testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003etestosterone cypionate which is the oil-soluble 17 (beta)-cyclopentylpropionate ester of the androgenic hormone testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEndogenous androgens are responsible for normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include growth and maturation of the prostate, seminal vesicles, penis, and scrotum; development of male hair distribution, such as beard, pubic, chest, and axillary hair; laryngeal enlargement, vocal cord thickening, and alterations in body musculature and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, and phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are responsible for the growth spurt of adolescence and for eventual termination of linear growth, brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth centers and termination of the growth process. Androgens have been reported to stimulate production of red blood cells by enhancing production of erythropoietic stimulation factor.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53717362999588,"sku":null,"price":540.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d8626239-5028-401b-b78e-0c8b7f8f7da9.jpg?v=1778005448"},{"product_id":"keifei-test-e-250","title":"Keifei Test E 250","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI T ENBOLIN 250(250MG\/ML TESTOSTERONE ENANTHATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 8 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic Steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-1000mg weekly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, high due to estrogen conversion\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes, normally due to high water \/electrolyte retention\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low in listed dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone was generally toted as the big daddy of injectable steroids. No other steroid was consistently reported to bring such high returns as quickly in weight gain and strength increases. Due to its high anabolic\/high androgenic effects, many athletes used this drug in an off-season mass cycle. Water retention during administration of ENANTHATE was not reportedly as high as that realized during the use of OMNADREN. but darn close. Like all testosterone esters, Enanthate aromatized easily and has a high conversion rate to DHT. Those with prostate problems or who were sensitive to gyno and female pattern fat deposits, readily agreed that they should have either left it alone or taken steps to suppress estrogenic activity due to aromatization.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrugs such as PROVIRON and NOVLADEX were often utilized for this reason. DHT\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003econversion enzyme blockers such as Proscar were commonly co-administered with testosterones for the former reason.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone enanthate notably suppressed HPTA function severely. HCG\/Clomid were considered almost a must to stimulate normal endogenous (natural) testosterone production within a positive period of time at post use. My personal experience has been that if a cycle containing testosterone enanthate lasted longer than 6 weeks, HCG and usually Clomid were introduced for 10 days beginning at the end of week #4. (5000 i.u. of HCG 3 times in 10 days usually normalized sperm and endogenous testosterone production to a respectable extent) Without the use of HPTA stimulating compounds normalization did occur, only at a much slower rate. For this reason, gains made during “enanthate only” administrations were not well maintained after use was discontinued, and much was lost needlessly by most regardless. Perhaps this was why so many uninformed individuals stayed on the stuff almost year round. (There are several solutions and protocols that prevented excessive post-cycle lean mass tissue loss for the more informed athletes)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales injected 200-1000mg weekly. Some did use much higher dosages of course. Due to a plasma half-life of 4-5 days, injections were normally administered bi­weekly. Most novice steroid should not use testosterone. Not only was considered unnecessary, it would have been foolish to diminish possible later gains when more gentle AAS were no longer providing results at reasonable dosages. Most users made excellent progress with a total weekly dosage of 200-600mg. Post-cycle use of an anti-catabolic drug was a constant agreed upon factor since it helped to maintain gains. (See Clenbuterol)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe negative side effects reported were mostly water retention and strong androgenic effects. These included gyno, accelerated hair growth, receding hair-lines, aggressiveness, higher blood pressure, acne, and increased fat deposits (due to aromatization). Since testosterones are metabolized by the liver fairly easily, alarming elevated liver enzymes occurred in very high dosages only. usually. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are derivatives of cyclopentano-perhydrophenanthrene. Endogenous androgens are C-19 steroids with a side chain at C-17, and with two angular methyl groups. Testosterone is the primary endogenous androgen.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn their active form, all drugs in the class have a 17-beta-hydroxy group. Esterification of the 17-beta-hydroxy group produces compounds (testosterone enanthate and testosterone propionate) which have a longer duration of action and are hydrolyzed in vivo to free testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are steroids that develop and maintain primary and secondary male sex characteristics.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEndogenous androgens are responsible for the normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include the growth and maturation of prostate, seminal vesicles, penis, and scrotum; the development of male hair distribution, such as beard, pubic, chest and axillary hair; laryngeal enlargement, vocal chord thickening, alterations in body musculature, and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are responsible for the growth spurt of adolescence and for the eventual termination of linear growth which is brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause a disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth center and termination of growth process.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens have been reported to stimulate the production of red blood cells by enhancing the production of erythropoietic stimulating factor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDuring exogenous administration of androgens, endogenous testosterone release is inhibited through feedback inhibition of pituitary luteinizing hormone (LH). At large doses of exogenous androgens, spermatogenesis may also be suppressed through feedback inhibition of pituitary follicle stimulating hormone (FSH).\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53735585972516,"sku":null,"price":540.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_b8d69406-3276-4dcd-b8e1-c0d79f7dee30.jpg?v=1778047116"},{"product_id":"keifei-anavar-100-tabs-10mg","title":"Keifei Anavar 100 Tabs 10mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI ANAVARBOL(10MG OXANDROLONE\/TAB=100TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 24\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 322-630\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD DIHYDROTESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 8-12 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic Steroid (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 20-50mg daily Women 10-15mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Only when administered in high dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes, c17-alfa-alkylated steroid. Due to low dosages toxicity is low-moderate\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: Quite low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Unlikely even in high dosage use\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone was often refereed to as an all purpose oral AAS. This drug was once marketed under the product name (still commonly used trade name) of Anavar. It has the unique quality of significantly stimulating (more than other AAS) the synthesis of phosphocreatine in muscle cells which in turn provides faster regeneration of, and a distinct elevation in, ATP. Of course all AAS have this effect to some extent. Oxandrolone is simply unmatched in this aspect.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e(See Creatine for more info) Due to this quality, a rapid build- up in strength was frequently reported and an obvious distinct hardness in muscle was obtained with little weight gain and no aromatization.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThough it is a common belief that Oxandrolone is not very anabolic, a clinical study showed a 44% increase in muscle cell protein synthesis after only 5 days of administration. Since Oxandrolone does not aromatize to estrogen, water retention is reported as quite low and gyno was of no concern. Also, for the same reason, during dieting phases fat deposits were said to be “burned away” more quickly. (Especially when the drug was co-administered with Clenbuterol).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone was reported to stack well with so -called mass steroids such as testosterone or with high anabolic\/moderate androgenic steroids such as Equipoise or Nandrolones. Persons over 40 have reported excellent results by stacking 15-25 mg of Oxandrolone daily with 200-400 mg of Deca.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA very hard pre-contest appearance has been achieved by males when stacked with Oxandrolone and Halotestin if a estrogen\/progesterone receptor antagonist (*See Nolvadex) had been utilized as well. As I said: “all purpose” was commonly the term of choice.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe drug Oxandrolone was originally manufactured to be used by women to prevent osteoporosis and for children as a cure for stunted growth. The low androgenic quality prevents almost all virilization for women in dosages of 15-mg daily or less. And for the same reason does not cause closure of the epiphysial plates prematurely. An interesting note: Oxandrolone does not suppress any part of the HYPOTHALAMUS-PITUITARY-TESTES AXIS (HPTA). This means Oxandrolone by itself will not significantly suppress natural testosterone production. Therefore it was not uncommon for some athletes to report post-cycle HPTA regeneration protocols that included this drug. The result was prominent lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdjunctive therapy to promote weight gain after weight loss following extensive surgery, chronic infections, or severe trauma, and in some individuals who, without definite pathophysiologic reasons, fail to gain or maintain normal weight; to offset protein catabolism associated with prolonged administration of corticosteroids; for relief of bone pain frequently accompanying osteoporosis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso used for Catabolic illness (eg, alcoholic liver disease, burn injury).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone 5 is typically used for\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCutting and hardening of skeletal muscles.\u003c\/div\u003e\n\u003cdiv\u003eThose who wish to loose weight without exercise.\u003c\/div\u003e\n\u003cdiv\u003eTreating muscle wasting diseases and osteoporosis.\u003c\/div\u003e\n\u003cdiv\u003eHelping burn victims regain muscle.\u003c\/div\u003e\n\u003cdiv\u003eContents per box:\u003c\/div\u003e\n\u003cdiv\u003e56 Green tablets in a labeled bag or labeled glass bottle.\u003c\/div\u003e\n\u003cdiv\u003eRecommended dose\u003c\/div\u003e\n\u003cdiv\u003eAlways take Oxandrolone 5 exactly as prescribed by your doctor. If you are unsure, ask your pharmacist. Unless otherwise prescribed by a doctor, the normal dose is:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMen\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFirst time users \u003c\/div\u003e\n\u003cdiv\u003eTake dose every 12 hours as follows: 20mg 30 minutes pre-training and 10mg 12 hours later for 2 weeks. Then increase daily dosage by 10 mg as follows: one 20mg 30 minutes pre training and two 10mg doses. These three doses to be taken at 8 hourly intervals.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdvanced users\u003c\/div\u003e\n\u003cdiv\u003eTake 20mg doses 4 times per day at 6 hourly intervals. Do not exceed 20mg per dose or 80mg per 24 hour period.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e Women\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFirst time users \u003c\/div\u003e\n\u003cdiv\u003eTake dose every 12 hours as follows: 5mg 30 minutes pre-training and 2,5mg 12 hours later for 2 weeks. Then increase daily dosage by 2,5mg as follows: 5mg 30 minutes pre training and two 2,5mg doses. These three doses to be taken at 8 hourly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDuration\u003c\/div\u003e\n\u003cdiv\u003eMinimum recommended duration is 6 weeks and maximum duration is 12 weeks\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737161720100,"sku":null,"price":1060.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_9d839d20-6c97-47ac-9d1c-792260a45f40.jpg?v=1778049280"},{"product_id":"keifei-clenbuterol-100-tabs-20mg","title":"Keifei Clenbuterol 100 Tabs 20mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI CLENBUTERIC(40MCG CLENBUTEROLHCL\/TAB=100TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: Up to 68 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Beta-2-symphatonimetic, thermalgenic\/anticatabolic (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 100-140 mcg per day Women 80-100 mcg per day\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Some reported high blood pressure\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Unknown Strong Anti-Catabolic\/Thermalgenic \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol is a quite strong anti-catabolic \/ thermalgenic drug that is not a steroid. During dieting periods, or post steroid cycles, this drug has reported dramatic effects on body composition. Since it suppresses the muscle wasting effects of cortisol\/cortisone, a slight increase in total muscle protein synthesis was seen. When stacked with steroids the effect were synergistic and more profound. When used as a post-cycle drug, clenbuterol helped to maintain muscle gains after AAS were discontinued. In both cases the drug acted to reduce fat deposits by elevation of thermalgenesis. It was considered very important to all polled whom had utilized this drug to start with 1-2 tabs daily (2 on -2 off) and monitor body temperature. (Increased dosages can increase body temperature to dangerous levels) Most obtained excellent results in 4-8 weeks. Many also stacked clenbuterol with thyroid drugs and \/or DNP to increase the rate of calorie expenditure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHeadaches, high blood pressure, and elevated body temperature were among noted side effects. Many reported side effects after 8-12 days. The body quickly adapts to clenbuterol so “on\/off” periods were a must for successful results. By alternating between E\/C (Ephedrine and caffeine) stacks and Clenbuterol, the effective period was extended and results increased. Rotations weekly such as clenbuterol, week #1, ephedrine\/ caffeine week# 2, seem to have brought superior results.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe reason clenbuterol begins to lose effectiveness after only 2 weeks is that the beta-2-receptors it interacts with are quite sensitive. (These are adrenalgenic receptors) Once these receptors are over stimulated for a prolonged period of time they become insensitive. Oddly enough it appears that DNP and thyroid hormones help regenerate adrenalgenic receptor function.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSince Clenbuterol dilates blood vessels in skeletal muscle but relaxes smooth muscle blood vessels, the physical reactions are quite similar to the body’s own epinephrine and can effect heart rate. It also reduces the level of the amino acid taurine in the heart which stabilizes cardiac rhythms, or the electrical activity in the heart. Increased intake for taurine during use was noted as wise.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMost bodybuilders don’t realize that the anabolic effects of Clenbuterol are not due to increased anabolic activity. Clenbuterol is actually effective through a different mechanism. It decreases both protein synthesis and break down. The reason anti-catabolic effects result is simply because it hinders protein break down more which shifts the ratio in favor of anabolism. This means that clenbuterol had significant anti-catabolic effects when stacked with a cortisol inhibitor post or during AAS cycles. Cytadren was an often noted example. Again, since clenbuterol increases thermalgenesis, (calories released as heat) the common use of thyroid T-3 or T-4 in a stack with it caused a significant increase in body temperature. This was monitored closely by most.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol is utilized to treat asthma in several countries. The dosage for treatment is normally 20-30 mcg\/d.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol Hydrochloride is a powerful bronchodilator that is used to treat breathing disorders like asthma. While it’s been extremely successful in such treatment plans it has never been approved by the U.S. FDA. It is, however, approved and used in most other countries around the world. Some speculate the only reason Clenbuterol has never been approved by the U.S. FDA is due to there being no need. There are several other related medications, very closely related that are already approved for U.S. use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol is commonly used as a thermogenic. You will find more Clenbuterol use in fat loss plans than anywhere else. It is very common fat burning tool used by many anabolic steroid users. It is a long standing favorite among competitive bodybuilders and other physique athletes during contest preparation. However, it is also used by non-steroid users for its fat loss properties. You do not have to use steroids to use clen for fat loss. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow Clenbuterol works\u003c\/div\u003e\n\u003cdiv\u003eAs a thermogenic, the effects of Clenbuterol are simple. As the body temperature increases, which is due to the beta-2 stimulation, the athlete is able to burn calories at an enhanced rate. As body temperature rises, the individuals metabolism is enhanced, fat cells are stimulated due to the increase in temperature and enhanced metabolism, the breakdown of triglycerides is now ocurs which results in loss occurs.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects of Clenbuterol\u003c\/div\u003e\n\u003cdiv\u003eSide effects or sides to Clenbuterol are as a result of its stimulant nature.. Mild side effects are jittering (Shakes) which can be mild to severe. Sweats and agitation are also common. Side effects will tend to be more pronounced when beginning a cycle and subside over time.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe more serious side affects of Clenbuterol Hydrochloridewhich are associated with high dosage and extended use, These include high blood pressure, irregular heartbeat, trembling and even panic. Some studies have also shown that Clenbuterol abuse can also lead to cardiac hypertrophy, which could potentially lead to death. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAt EU Pharmaceuticals responsibility and Safe are our motto which is why we recommend short cycles of Clenbuterol for Fat burning at low dose which carry a lower risk.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFat Burning Cycle for Clenbuterol\u003c\/div\u003e\n\u003cdiv\u003eTwo weeks on 2 weeks off at 20mcg – 60mcg per day ( half to 1.5 tablets)\/ day\u003c\/div\u003e\n\u003cdiv\u003estart at half a tablet per day and increase dosage as you adapt. Always err on the lower dosage side\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eContinuous usage for 6 – 8 weeks\u003c\/div\u003e\n\u003cdiv\u003eStart at low dose of 20 mg- 40 mg dependent on your ability to cope with the product ( always start at a a lower dose) increase dosage by 20mcg everyday until max of 140mcg for men (3.5 tablets) and 120mcg (3 tablets) for woman.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eShort cycle 2 – 3 weeks\u003c\/div\u003e\n\u003cdiv\u003eStart at 40mcg and increase till maximum required over first week and hold for remainder of cycle\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol Product Description\u003c\/div\u003e\n\u003cdiv\u003eEU Pharmaceuticals brand Clenbuterol is packaged in 2 blisters each containing 28 tablets. 2 blisters per box = 56 tablets in a box at a dose of 40mcg\/tablet\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737288565028,"sku":null,"price":380.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_bede0b94-2183-4989-b1d5-0c3eafe7e955.jpg?v=1778049448"},{"product_id":"keifei-dianabol-10mg","title":"Keifei Dianabol 10mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI DIANABOL(10MG METHANDIENONE\/TAB=100TABS) \n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 40-60\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 90-210\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 6-8 hours (Injection product remains active for about 60-72 hours) Drug Class:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnabolic\/androgenic steroid ORAL OR INJECTABLE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 15-50 mg daily Women 5-10 mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes, especially in higher dosages.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, similar to testosterone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes, due to water retention, some experience elevated heart rate\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, strongly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes, 17-alfa alkylated oral\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh anabolic\/high androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Yes, dose and administration period dependent\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOral Dianabol was reported to be a highly effective mass AAS which provided impressive weight and strength gains. Most users experienced a 2-4 LB bodyweight increase per week with heavy water retention. With higher dosages gynecomastia (bitch tits) was a common negative side effect. Obviously much of this was avoided by those who reported co-addministration of Proviron and\/or Novladex. When stacked with a nandrolone, some gyno problems seemed to lessen. This was probably due to Nandrolones aromatization to a weaker estrogen called Norestrogen and the resulting mild anti-estrogenic effect that results in moderate dosage administration. Methandrostenlone becomes active in 1-3 hours with a half-life of about 3.5-4.5 hours. For this reason, dosages were spread through out the day to maintain blood serum\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003econcentrations at an elevated state. Massive dosages just were not necessary since a single 10-mg dose has increase androgen anabolic activity 5 times over normal with a correlating reduction in natural cortisol activity of 50-70%. Males using 5mg per 25-LBS of body weight broken into 3-5 equal dosages throughout the day have experienced impressive results. At dosages above 50 mg per day, results were not progressively quantitative. Most first time AAS users who used a daily dosage of 20-30mg daily experience significant results over a 4-6 week period. Women should not utilize Methandrostenolone but a surprising number did report the inclusion of the drug in AAS protocols. For those who insisted, no more than 10-mg daily for 3-4 weeks stacked with a very low androgenic product minimized masculization type negative side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects such as increased liver values (toxicity) “usually” returned to normal within a short period of time after use was discontinued. High blood pressure, elevated heart rates, gyno, heavy water retention, and acne were all frequent reported negative side effects of Methandrostenlone use. Some literature on this drug supports DHT- like activity. Finasteride “usually” prevented this effect as well as possible prostate enlargement. Dianabol heavily suppresses natural testosterone production within only 10 days after continuous administration begins (dose dependent). Most note a sense of well being during use of this drug. Significant strength and weight loss follows discontinued use due to the loss of excessive water and HPTA suppression. So retained gains were only fair post-cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMy personal experiences with this drug have led me to believe that no athlete should have ever stacked high dosage protocols of Dianabol with Anadrol-50 or Methyltestosterone. It is a liver killer combo. A last note: Injectable Dianabol did not have anywhere near as dramatic effects when utilized in its intended method. However, the injectable is orally active and as such was reported to be commonly used in this manner by filling gel-caps with the desired amount\/dosage and subsequent ingestion. This is probably due to the fact that oral administration of a c17-alkylated AAS results in increased liver production of IGF-1. I have also learned that it was best to avoid Russian Methandrostenlone. (It commonly contains a large amount of unconverted methyltestosterone).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003emethandrostenolone does not react strongly with the androgen receptor , instead relying on activity not mediated by the receptor for its effects. These include dramatic increases in protein synthesis , glycogenolysis , and muscle strength over a short space of time. . In high doses (30 mg or more per day), side effects such as gynaecomastia , high blood pressure , acne and male pattern baldness may begin to occur. The drug causes severe masculinising effects in women even at low doses. Without the administration of aromatase inhibitors such as Arimadex , estrogenic effects will appear over time in men. Many users will combat the estrogenic side effects with Tamoxiplex or Clomid . \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe 17α-methylation of the steroid does allow it to pass through the liver without being broken down allowing it to be taken orally. It also has the effect of decreasing the steroid’s affinity for sex hormone binding globulin , a protein that de-activates steroid molecules and prevents them from further reactions with the body. As a result, methandrostenolone is significantly more active than an equivalent quantity of testosterone , resulting in rapid growth of muscle tissue. However, the concomitant elevation in estrogen levels – a result of the aromatization of methandrostenolone – results in significant water retention. This gives the appearance of great gains in mass and strength, which prove to be temporary once the steroid is discontinued and water weight drops. Because of this, it is often used by bodybuilders only at the start of a “steroid cycle”, to facilitate rapid strength increases and the appearance of great size, while compounds such as Testosterone or Deca with long acting esters build up in the body to an appreciable amount capable of supporting anabolic function on their own.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDianabol 20 is typically used for:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e“Kick starting” bulking cycles.\u003c\/div\u003e\n\u003cdiv\u003e“Bridging” between cycles to maintain gains.\u003c\/div\u003e\n\u003cdiv\u003eA beginners bulking cycle.\u003c\/div\u003e\n\u003cdiv\u003eContents per box:\u003c\/div\u003e\n\u003cdiv\u003e56 Red tablets in a labeled bag or labeled glass bottle.\u003c\/div\u003e\n\u003cdiv\u003eRecommended dose\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlways take Dianabol 20 exactly as prescribed by your doctor. If you are unsure, ask your pharmacist. Unless otherwise prescribed by a doctor, the normal dose is:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMen\u003c\/div\u003e\n\u003cdiv\u003eFirst time users:\u003c\/div\u003e\n\u003cdiv\u003eTake a 10mg dose twice a day as follows: 10mg in the morning and 10mg in the evening for 2 weeks. Then increase daily dosage by 10 mg as follows: one 10mg dose three time per day spread evenly throughout the day.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdvanced users:\u003c\/div\u003e\n\u003cdiv\u003eTake one 20mg dose three time per day spread evenly throughout the day. Do not exceed 20mg per dose or 60mg per 24 hour period.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen\u003c\/div\u003e\n\u003cdiv\u003eTake 10mg once per day in the morning. Then increase daily dosage by 10mg as follows: one 10mg dose twice a day 10mg in the morning and 10mg in the evening.\u003c\/div\u003e\n\u003cdiv\u003eAs Dianabol 20 only comes in 20mg capsules, it’s advised that the tablet is halved on the break line.\u003c\/div\u003e\n\u003cdiv\u003eDuration\u003c\/div\u003e\n\u003cdiv\u003eMinimum recommended duration is 6 weeks and maximum duration is 12 weeks\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737345286436,"sku":null,"price":420.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_3329f595-5f2f-4b28-a951-f216829bf5af.jpg?v=1778049549"},{"product_id":"keifei-primabolin-100","title":"Keifei Primabolin 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI PRIMABOLIN 100(100MG METHENOLONE ENATHATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 44-57\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 88\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 10-14 DAYS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic Steroid (Oral) OR (FOR INJECTION)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-400-mg weekly Women 50-150-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Light at dosages of up to 200-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Very low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases: HPTA function: Only slightly in dosages over 300mg weekly and due to prolonged periods of use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimobolan Depot is similar to the acetate tablets with a few differences. Though it is a predominantly anabolic steroid, being a DHT derivative it also maintains some androgenic qualities. For this reason, it does have virilizing aspects to consider. This explains the improved strength and harder appearance polled users obtained in part. Naturally since it does not convert to estrogens, induced low water retention and a distinct lack of gyno and female pattern fat deposits was noted as avoided. In fact, the drug does theoretically act as an anti-estrogen to a lesser extent.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Women reported they were able to avoid some virilizing aspects with Proscar.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMost first time male (AAS novices) users reported an 8-16 lb gain after 6-8 weeks of 200mg weekly dosages. The new muscle was of a high quality and usually was retained quite well after discontinuance. This may have been due to Primobolan depot having only a slight negative effect upon the Hypothalamic-Pituitary-Testes-Axis (HPTA). In short, this drug was noted to only slightly shut down natural testosterone production and therefore there was not a significant lack of testosterone or an elevation in circulatory estrogen post- cycle. This was especially true if dosages were kept at 200-300-mg weekly for no more than 6-8 weeks for males. (Women don’t have testes, remember?). For this reason, older males made excellent and reasonably permanent gains with little interruption in their already lower natural androgen production. For stacks focusing on this issue, Oxandrolone and Android were said to work very well with Primobolan Depot. Primobolan based stacks containing nandrolones and\/or Equipoise were commonly utilized for this purpose also.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*A point of interest: Primobolan Depot (like Winstrol Depot) has been noted to possess excellent site- injection qualities. This means that a lagging body part became the injection site for dosages. Most who used this type of\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen actually should not have used high dosages of any DHT product or derivative. DHT has excellent hardening effects, but also has masculinizing aspects. An often noted as safer method for use of such drugs was to also co-administer a 5-ALFA-REDUCTASE INHIBITOR such as Proscar. Its active ingredient is Finasteride which blocks testosterone’s conversion to DHT. Yes, that is the pill guys take to stop their hair -line from receding. 1mg daily was said be enough when women stayed in the 50-200mg weekly dosage range when using Primobolan Depot.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSince Primobolan Depot actually has an active-life of closer to two weeks, injections were commonly administered weekly by those whom reported lower dosage use. But due to predominantly 50-mg\/ml ampules being the most available a 4-ml\/200mg injection “hurt” to an excessive degree for those whom employed the higher dosage protocols. So twice weekly injections was the normal method chosen.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*It was my experience that Primobolan was one of the few steroids capable of increasing lean mass during calorie restricted periods therefore remaining effective even in calorie deficit induced catabolic environments. This drug is an Enanthate ester and should provide an 8 day active life. Strangely enough it does provide the above listed active-life range though the ester is an enanthate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimo 100 for intramuscular injection, contains methenolone enanthate\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMethenolone Enanthate is a DHT based anabolic steroid. When it interacts with the aromatase enzyme it does not form any estrogens. It is used by people who are very succeptible to estrogenic side effects, having lower estrogenic properties than Nandrolone. Methenolone is available as an injection or as an oral. The injection is naturally regarded as having a higher bioavailability. Its an enanthate ester which is quite long-acting. Because it by-passes hepatic breakdown on the first pass, it also has a higher survival rate. The tablets are in a short-lived acetate form. Methenolone is not 17-alpha-alkylated, but 1-methylated for oral bioavailability. This reduces the stress on the liver, but also the availability. It is considered one of the safer steroids, meaning it has a very little side effects. Methenolone has no estrogenic side effects, and its effects on cholesterol levels are minimal. In doses of 200 mg or less (intramuscular) blood pressure is rarely altered.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePossibly one of the safer anabolic steroids for females due to very low virilization effects in short-term usage. Of course, this is not a blanket-statement and individual results (dependent on doses and tolereance) will vary.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMethenolone is also not overly suppressive of the HPTA axis, although how suppressive is debatable. For this reason, many bodybuilders use it in between steroid cycles during their “off-time” to help maintain their gains and strength. The long term safety of such a practice possibly dangerous and can lead to permanent suppression of the HPTA.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737395716388,"sku":null,"price":1330.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_3848d591-4fe0-4581-9020-11063662497a.jpg?v=1778049643"},{"product_id":"keifei-winstrol-100-tabs-10mg","title":"Keifei Winstrol 100 Tabs 10mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cdiv\u003e\u003cspan\u003eKEIFEI STANABOL(10MG\/TAB STANOZOLOL=100TABS) \u003c\/span\u003e\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eORAL VERSION\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 30\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 320\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD METHYLTESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 8 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Males 20-50-mg daily Women 10-15-mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: High in high oral dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: None, DHT derivative\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePretty much everything written thus far about Stanozolol injectable (*See “Winstrol Depot” under “Injectable Anabolic Androgenic Steroids” for more info) was also attributed also to the oral form. It was often said that the oral form is less effective than the injectable. In truth, it was usually due to dosages, and this in turn was due to price. Athletes usually administered a lower dosage orally because it seemed like 25 pills daily was mega dosing. In my personal opinion this was true to a point. Oral use of any 17-alfa-alkylated steroid is hard on the liver. This is because it is difficult for the liver to deactivate these modified testosterone and derivatives. Let me make it clear. Milligram for milligram oral administration of Stanozolol was reported significantly more potent than the injection product (but it is more liver toxic). Oral dosages were commonly broken into 2-3 daily dosages to maintain circulatory androgen elevation. An effective reported daily oral dosage for women was 10-15mg and for men 20-30. However, this listed male dosage was not as effective (or as toxic) as the 30-50mg daily dose range.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMale athletes reported the practice of stacking 40-50mg of Stanozolol daily with 300-400mg weekly of a nandrolone provided significant lean muscle tissue augmentation with good post-cycle retention. For “bulking” purposes many reported the use of this drug with a testosterone at an average reported dosage of 200-600mg weekly resulted in “amazing strength and weight gains” and improved post-cycle lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen athletes commonly reported the use of Stanozolol at a dosage of 10-15mg daily with 50-100mg of a nandrolone weekly resulted in a rapid increase in quality lean mass tissue with low water retention and rare virilizing negative side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnabolic steroids such as Stanozolol are synthetic derivatives of the male hormone testosterone. Stanozolol has a pronounced anabolic effect with fewer masculinizing side effects than testosterone and some other synthetic anabolic steroids. Anabolic steroids are used in stimulating appetite and increasing weight gain, strength, and vigor. They should be used as a part of an overall program with other supportive and nutritional therapies.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is a very popular anabolic steroid, which is a derivative of dihydrotestosterone. Winstrol is a relatively low androgenic steroid which will not aromatise. It is moderately toxic to the liver. Very few users report any water retention or any other side effects while using Winstrol. It is a popular drug for cutting in a stack with Primobolan or Parabolan. When stacked with Testosterone it can be very effective for a size and strength gain. Women use the drug quite often, but it can cause virilising effects for some women even at low dosages. Most of the muscle gains made while taking the Winstrol are retained after the drug is discontinued. The injectable form is better than the oral. Many feel that the injectable must be administered at least twice a week: some take shots every day for better effects. Dosages range from 3 to 5 cc?s per week for men, 1 to 2 cc’s in women. .\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is used in the treatment of hereditary angioedema.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud’s disease, vasculitis of Behcet’s disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozol 20 is typically used for\u003c\/div\u003e\n\u003cdiv\u003eA cutting cycle\u003c\/div\u003e\n\u003cdiv\u003eLowering SHBG\u003c\/div\u003e\n\u003cdiv\u003eContents per box:\u003c\/div\u003e\n\u003cdiv\u003e56 bright blue tablets, sealed in a labelled bag or bottle. Please note unique hologram for authenticity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eRecommended dose:\u003c\/div\u003e\n\u003cdiv\u003eAlways take Stanozol 20mg exactly as prescribed by your doctor. If you are unsure, ask your pharmacist. Unless otherwise prescribed by a doctor, the normal dose is as follows:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFor Men:\u003c\/div\u003e\n\u003cdiv\u003eFirst time users\u003c\/div\u003e\n\u003cdiv\u003eTake a 20mg dose twice a day as follows:10mg in the morning and 10mg in the evening for 2 weeks. Then increase daily dosage by 10 mg as follows: one 10mg dose three time per day spread evenly throughout the day.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdvanced users\u003c\/div\u003e\n\u003cdiv\u003eTake one 20mg dose three time per day spread evenly throughout the day. For lowering SHBG The use of 0,2mg\/kg body weight per day dramatically lowers SHBG which in turn increases the amount of free testosterone circulating in the body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDo not exceed 20mg per dose or 60mg per 24 hour period.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHalf Life for this product is 9 hours.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdvanced users\u003c\/div\u003e\n\u003cdiv\u003eTake 20mg doses 3 times per day at 8 hourly intervals. Do not exceed 20mg per dose or 60mg per 24 hour period.\u003c\/div\u003e\n\u003cdiv\u003eStanozol 20mg is to be taken with food to avoid stomach irritability, this may however diminish bioavailablity of the product. Therefore, fatty foods in particular should be avoided 1 hour prior to dose administration. It is not advised but you may also take Stanozol 20mg without food.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIncrease your water intake to avoid kidney \/ liver related side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDuration:\u003c\/div\u003e\n\u003cdiv\u003eMinimum recommended duration is 4 weeks and maximum duration is 8 weeks. There are however reports of people using Stanozol 20 for up to 12 weeks without complication.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePossible side effects include, but are not limited to, stiffening of joints \/ joint pain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eShould this occur; please lower your dosage, if taking a high dose, or discontinue usage.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eORAL VERSION\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 30\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 320\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD METHYLTESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 8 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Males 20-50-mg daily Women 10-15-mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: High in high oral dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: None, DHT derivative\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePretty much everything written thus far about Stanozolol injectable (*See “Winstrol Depot” under “Injectable Anabolic Androgenic Steroids” for more info) was also attributed also to the oral form. It was often said that the oral form is less effective than the injectable. In truth, it was usually due to dosages, and this in turn was due to price. Athletes usually administered a lower dosage orally because it seemed like 25 pills daily was mega dosing. In my personal opinion this was true to a point. Oral use of any 17-alfa-alkylated steroid is hard on the liver. This is because it is difficult for the liver to deactivate these modified testosterone and derivatives. Let me make it clear. Milligram for milligram oral administration of Stanozolol was reported significantly more potent than the injection product (but it is more liver toxic). Oral dosages were commonly broken into 2-3 daily dosages to maintain circulatory androgen elevation. An effective reported daily oral dosage for women was 10-15mg and for men 20-30. However, this listed male dosage was not as effective (or as toxic) as the 30-50mg daily dose range.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMale athletes reported the practice of stacking 40-50mg of Stanozolol daily with 300-400mg weekly of a nandrolone provided significant lean muscle tissue augmentation with good post-cycle retention. For “bulking” purposes many reported the use of this drug with a testosterone at an average reported dosage of 200-600mg weekly resulted in “amazing strength and weight gains” and improved post-cycle lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen athletes commonly reported the use of Stanozolol at a dosage of 10-15mg daily with 50-100mg of a nandrolone weekly resulted in a rapid increase in quality lean mass tissue with low water retention and rare virilizing negative side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnabolic steroids such as Stanozolol are synthetic derivatives of the male hormone testosterone. Stanozolol has a pronounced anabolic effect with fewer masculinizing side effects than testosterone and some other synthetic anabolic steroids. Anabolic steroids are used in stimulating appetite and increasing weight gain, strength, and vigor. They should be used as a part of an overall program with other supportive and nutritional therapies.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is a very popular anabolic steroid, which is a derivative of dihydrotestosterone. Winstrol is a relatively low androgenic steroid which will not aromatise. It is moderately toxic to the liver. Very few users report any water retention or any other side effects while using Winstrol. It is a popular drug for cutting in a stack with Primobolan or Parabolan. When stacked with Testosterone it can be very effective for a size and strength gain. Women use the drug quite often, but it can cause virilising effects for some women even at low dosages. Most of the muscle gains made while taking the Winstrol are retained after the drug is discontinued. The injectable form is better than the oral. Many feel that the injectable must be administered at least twice a week: some take shots every day for better effects. Dosages range from 3 to 5 cc?s per week for men, 1 to 2 cc’s in women. .\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is used in the treatment of hereditary angioedema.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud’s disease, vasculitis of Behcet’s disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737506603300,"sku":null,"price":440.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c3429730-8361-434d-9e83-a425dfa26322.jpg?v=1778049775"},{"product_id":"keifei-deca-250","title":"Keifei Deca 250","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eChemical Name: Nandrolone Decanoate\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: 250mg\/ml x 10ml multi doses vial and 250mg\/ml x 1ml single dose ampoule\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePresentation: 10ml multi dose clear vial with Keifei® wording imprinted on the side. 10ml x Nandrolone decanoate 250mg\/ml. Sealed with yellow flip off cap imprinted with keifei® wording. Each vial comes with 1 sets of 10 digits authentication codes. 10 vials\/ box in a white and yellow colour outer box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e1ml single dose ampoule x Nandrolone decanoate 250mg\/ml. Each ampoule imprinted with 3 rings on top Brown, yellow, Brown with a Black dot below. All wording is imprinted. Pack in 3 ampoules or 10 ampoules of 5 ampoules per tray x 2 in plastics insert with Keifei® imprint on it.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe outer box contains 60ampoules of 20 inner boxes of 3 Ampoules in a White and Yellow box. Each inner box pack of 3 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOr the outer box contains 100 ampoules of 10 inner boxes of 10amps in white and yellow box. Each inner box pack of 10 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* Remarks: NEW PACKING WITH IMPROVE QUALITY AND QC CHECK UNDER USP STANDARD, KNOW AS KEIFEI® PHARMA.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* Keifei Pharma rubber stopper do not have keifei wording imprint on it.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNANDROLIN 250 – This ester said to be a slow release and super long acting compound. NANDROLIN 250 is one of the most widely used anabolic steroids. Its popularity is due to the sample fact that it produces many favorable properties. It is weaker than testosterone but the fact is NANDROLIN 250 will break down to more potent metabolite in androgen target tissue. There for it is far less likely to cause unwanted androgenic side effect. Basic androgenic side effects are oily skin, acne, body or facial hair growth, aggression and accelerated hair loss.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNANDROLIN 250 is not known as a very fast builder. The muscle building effect of this drug is quite noticeable, but not dramatic. The show onset and mild properties of this steroid therefore make it more suitable for cycle with longer duration. In general one except to gain muscle weight at about half the rate of that with an equal amount of testosterone use. Side effect are mild due to liver can convert Nandrolone to estradiol. But there are still some strong occurrences oily skins, acne, body or facial hair growth, and hair loss are very rare\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737635774756,"sku":null,"price":790.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_5493eba4-2088-4b11-baf4-5c07309b31f5.jpg?v=1778049925"},{"product_id":"keifei-masteron-e-200","title":"Keifei Masteron E 200","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cspan\u003eStrength\u003c\/span\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMuscle Gain\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFat\/Water Loss\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eKeep Gains\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: 200 mg – 400 mg \/ week\u003c\/div\u003e\n\u003cdiv\u003eChemical Name: Drostanolone propionate\u003c\/div\u003e\n\u003cdiv\u003eQuantity: 10ml vial\u003c\/div\u003e\n\u003cdiv\u003ePicture may differ from actual Product.\u003c\/div\u003e\n\u003cdiv\u003eCategories: All Injectables, All Products, Keifei Pharma, Keifei Pharma Injectables\u003c\/div\u003e\n\u003cdiv\u003eTags: Buy Keifei, Drostanolone Enanthate, Injectable oils, kiefei, Masterbolin, masteron E, steroids\u003c\/div\u003e\n\u003cdiv\u003eBrand: Keifei Pharma\u003c\/div\u003e\n\u003cdiv\u003eMasteron Enanthate, which should be more properly known as Drostanolone Enanthate, is a long estered variant of Drostanolone. Drostanolone was originally marketed on the prescription drug market under the brand name Masteron, which was Drostanolone Propionate (a short estered variant of Drostalonone. The trade name of Masteron caught on very quickly across bodybuilding circles, and the two should really be referred to as “Drostanolone Propionate” and “Drostanolone Enanthate” due to the fact that the brand name Masteron is really a descriptor for Drostanolone Propionate, and only Drostanolone Propionate. However, the Masteron trade name has stuck permanently onto the lips of bodybuilders and athletes everywhere, and so the Enanthate variant of Drostanolone is now referred to all the time as Masteron Enanthate. Chemically, the difference between Masteron Propionate and Masteron Enanthate is very much the exact same as the difference between Testosterone Propionateand Testosterone Enanthate. The base hormone, which in this case is Drostanolone, is affixed with an Enanthate ester on its 17-beta hydroxyl group.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe origins of Masteron Enanthate are not very clear at all. It is completely clear, however, that this is not and never ever was a pharmaceutical human grade product at all. Unlike similar products such as Trenbolone Enanthate that can be traced back to its first manufacture under specific underground labs (British Dragon), Masteron Enanthate has a far more shrouded history. It is currently unknown which underground labs, if any, originally introduced this product into the black market. There is some rumor that an underground lab by the name of Dpharm originally brought it into the market, but there is very little factual evidence to support these small rumors. Furthermore, it is not even entirely known when Masteron Enanthate hit the black market, though it was most likely during the early 2000s. This might make logical sense, considering the early 2000s was a period where a handful of underground laboratories (UGLs) were attempting to make headway into developing anabolic steroids that are beyond the scope of pharmaceutical application. Obviously the very first Masteron product (Masteron Propionate) entered the bodybuilding and athletic world by way of trickle-down from the pharmaceutical environment, but Masteron Enanthate seems to be a derivative resultant of the black market and underground world.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron Enanthate is not even commonly listed in many anabolic steroid reference books either, demonstrating just how rare and infrequent the status and history is of this drug. Being that it never ever was even developed or tested in the pharmaceutical drug world, there is literally zero clinical data, nor any mention in any scientific literature of this drug to go by. Masteron (Drostanolone Propionate) was developed in 1959 by Syntex[1] and immediately upon release to the prescription market it was used almost exclusively for the treatment of female breast cancer patients. It eventually hit the bodybuilding and athlete steroid-using circles towards the 1970s – 1980s, and consequently during the 1980s all forms of Masteron were eventually pulled from the prescription market and discontinued. Masteron Propionate today is no longer manufactured as a pharmcaceutical grade product, and Masteron Enanthate was never even on the list of medicines produced by any pharmaceutical firms, ever. Masteron Propionate gained significant popularity towards the 1980s and 1990s and onwards, which is perhaps why eventually towards the early 2000s Masteron Enanthate came to fruition. Ultimately the same thing occurred with many similar anabolic steroids that started off as short-estered compounds and later were offered as long estered compounds of underground origin (such as Trenbolone).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTo this day, however, the Propionate variant of Masteron remains the most commonly utilized and most popular variant, though the numbers of anabolic steroid users who now use Masteron Enanthate have increased substantially since the entrance of this product in the early 2000s on the black market.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat Is Masteron Enanthate and Why Is It So Popular?\u003c\/div\u003e\n\u003cdiv\u003eLet us start with the basics of the Drostanolone molecule itself. Drostanolone is a Dihydrotestosterone (DHT) derivative, meaning it is a modified form of DHT itself. There are many anabolic steroids within the family of DHT derivatives, some of which are very well known and very popular. DHT derivatives include: Anavar (Oxandrolone), Winstrol (Stanozolol), Primobolan (Methenolone), and various others. There is a good reason as to why DHT derivatives are very popular, very useful, and very effective compounds. Before expanding upon that, returning to Masteron (Drostanolone), Drostanolone differs from its parent hormone DHT by way of the addition of a 2-methyl group to its chemical structure. This makes Masteron significantly stronger in terms of anabolic effects compared to its parent hormone. However, although its anabolic properties are significantly greater when compared to its parent hormone, the anabolic properties when compared to most other anabolic steroids are modest at best. Because of this, Masteron is normally utilized as a fat loss, cutting, and most commonly, a pre-contest agent for the competitive bodybuilder. Masteron also has its place with athletes in the department of speed sports due to its ability to increase lean mass without any water retention, and in fact reduces water weight.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhich brings us to the next important property of Masteron: it has demonstrated capabilities of as a moderate aromatase inhibitor, as well as possibly acting to block Estrogen at receptor sites on breast tissue[2] [3]. This does make perfect sense when we see how the Propionate variant of Masteron was utilized exclusively within medicine to treat Estrogen-dependent breast cancer in females. Through its activity as an aromatase inhibitor, it can indeed cause a reduction in water through anti-estrogenic action. This is indeed the reason as to why at very low bodyfat percentages, bodybuilders experience a ‘chiseling’ and 3D ‘ripped’ look to the physique that is almost unique with Masteron. Finally, in addition to the chemical modifications, Masteron Enanthate has been affixed with the Enanthate ester on its 17-beta hydroxyl group, which serves to extend the half-life of the drug to about 7 – 10 days in the body. This is in contrast with Masteron Propionate, which is affixed with the Propionate ester and extends its half-life to that of a shorter duration: 4.5 days.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe reason as to why DHT-derivatives are so popular and useful in the world of bodybuilding and athletics is due to the fact that they are incapable of conversion (aromatization) into Estrogen. DHT is not recognized as a proper substrate for the aromatase enzyme in the body, and therefore any hormone that is derived from DHT will assume these same qualities. The only strange exception to this rule would be Anadrol-50 (Oxymetholone), which expresses heavy estrogenic effects, but still does not actually aromatize. On the other hand, no estrogenic effects what so ever should be experienced with the use of Masteron Enanthate at any dosage used at all. The same goes for any other compounds that are in the DHT-derivative family (with the exception of Anadrol, of course).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow Does Masteron Enanthate Work and How Is It Best Used?\u003c\/div\u003e\n\u003cdiv\u003eMasteron Enanthate is a long estered (and therefore, long acting) variant of Masteron, and is therefore best utilized in the context of longer cycle lengths (upwards of 10 – 12 weeks or longer). It is best used in cutting cycles, and even better for pre-contest cycles for competitive bodybuilders. Those who are looking for any significant strength gains or to bulk up on Masteron Enanthate will be greatly disappointed, as this is one anabolic steroid that is not deemed as very impressive in the area of anabolic strength, and in some cases might be weaker in strength than Testosterone. Masteron’s anabolic rating is that of 63 – 130. Testosterone’s anabolic rating by comparison is 100. We can see here that Masteron is at worst, about 30% weaker than Testosterone’s anabolic capabilities, and at best it is 30% stronger than Testosterone in this regard (where receptor binding affinity is concerned). So, while one could definitely experience satisfying results from Masteron Enanthate, it would by no means elicit an impressive or anywhere near dramatic response in an individual. Furthermore, Masteron Enanthate is best utilized in conjunction with other anabolic steroids. It’s solitary use alone might yield disappointment for the user, especially if the individual is not a bare beginner or first-time anabolic steroid user.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron Enanthate dosage requirements do not need to be that high, but it is recommended to begin (and normally maintain) around 400mg weekly. Ultimately, it is dependent almost completely on what the individual wishes to gain from the cycle and the compound itself. Beginner Masteron Enanthate dosage normally begins at the aforementioned 400mg\/week zone, though many bodybuilders who utilize it only for its anti-estrogenic or pre-contest effects could easily utilize 200mg\/week on top of other compounds. If the individual’s bodyfat percentage is low enough in this case, there should be significant aesthetic benefits to the physique even in the dosage range of 200mg\/week. Intermediate and advanced Masteron Enanthate doses as high as 600mg\/week or higher (800mg\/week or more) can be used, but are almost entirely unnecessary. Those who wish to gain significant amounts of strength and size from Masteron Enanthate would have to venture that high, but considering the expensive nature of this compound and its capabilities, it would be a waste to use Masteron Enanthate for a purpose such as mass and strength gaining. Furthermore, the capabilities of Masteron is understood by nearly all bodybuilders to be an aesthetic enhancement one – not a significant performance enhancement one, and certainly not a significant size and strength gaining one either.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStacking other anabolic steroids with Masteron Enanthate normally entail the use of other similar compounds, often tailored and geared towards the same goals and purposes. As a general rule of course, Testosterone should be utilized alongside any anabolic steroid. Naturally, the best choice to be utilized with Masteron Enanthate would be Testosterone Enanthate for obvious reasons. For those unaware of why, the combination of two Enanthate-based anabolic steroids merely make administration and timing of injections far more convenient and much easier. Following this, if any individuals wish to throw a third compound into the stack, there are some great choices to be made. A third compound could be an oral anabolic steroid, such as Winstrol or Anavar – both well suited towards the same type of goals that Masteron is as well. Alternatively, the use of a third injectable might be preferential for those especially serious or competitive. The best and most effective choice to run alongside Testosterone Enanthate and Masteron Enanthate would be Trenbolone Enanthate. This ‘Enanthate trio’ of Testosterone\/Drostanolone\/Trenbolone is regarded by many as the pinnacle cycle of competitive bodybuilders and pre-contest cycles. Obviously, all Enanthate variants are selected due to their great compatibility, and the intense anabolic effects of Trenbolone contribute exquisitely to the aesthetic enhancing effects of Masteron on the physique. Furthermore, neither Trenbolone nor Masteron aromatize into Estrogen at any dosage used. This, alongside the physique altering effects of Trenbolone and Masteron, allow the individual to effectively transform their physique within record time and beyond anything that can be imagined, which is why it is commonly utilized as a pre-contest cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron Enanthate is very rarely used in bulking or strength cycle stacks, and if done so, is normally used for its anti-estrogenic aromatase inhibiting properties. Even with such advantageous properties, many would conclude that such a use for Masteron is a waste of money, as much stronger anti-aromatase capability can be obtained for much cheaper by purchasing and using any of the commonly used aromatase inhibitor ancillary drugs.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron Enanthate Side Effects\u003c\/div\u003e\n\u003cdiv\u003eMasteron Enanthate is known for having quite a positive safety and tolerance record, although with it being an anabolic steroid by nature, there are some Masteron Enanthate side effects to be aware of and watch out for.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFirst and foremost, it is important to mention that there is no risk what so ever of any Estrogen related side effects from Masteron Enanthate alone. As mentioned previously, Masteron Enanthate not only avoids aromatization into Estrogen completely, but it even acts as an anti-Estrogen in many cases. Therefore, the typical estrogenic side effects that result from the use of aromatizable anabolic steroids is avoided. This includes: bloating, water retention, blood pressure increases (as a result of water retention), acne, and gynecomastia. Because of Masteron’s anti-estrogenic properties, it can actually help prevent or mitigate these side effects if they are occurring from other anabolic steroids that do aromatize.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogenic Masteron Enanthate side effects are a concern, and might be more so with Masteron than other anabolic steroids. Being a DHT-derivative, Masteron has the capability of being somewhat on the more androgenic side, and those who are sensitive to androgenic side effects should bear this in mind. Androgenic side effects include: increased oily skin, acne, increased aggression\/irritability, benign prostatic hyperplasia (BPH), and male pattern baldness if the genetic predisposition for it exists in the individual. An important note here is that 5-alpha reductase inhibitors such as Proscar, FInasteride, Dutasteride, or Propecia will do absolutely nothing to prevent the androgenic Masteron Enanthate side effects from occurring due to the fact that Masteron Enanthate does not undergo reduction into a more androgenic form in the body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBeing an anabolic steroid, Masteron Enanthate will suppress and possibly shut down the HPTA (Hypothalamic Pituitary Testicular Axis) through the negative feedback loop. This results in diminished or completely halted endogenous natural Testosterone production in the individual, and can persist even after the cycle is halted. If left untreated, it can leave the individual with a condition known as hypogonadism, whereby Testosterone production is impaired indefinitely. Performing a proper PCT program can increase the chances that this does not develop and that upon cessation of the cycle, the HPTA returns to normal functioning once again.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNegative cardiovascular issues are indeed a part of Masteron Enanthate side effects, and might be an even greater concern with Masteron Enanthate considering its anti-estrogenic properties. In particular, this impacts the levels of HDL (good) and LDL (bad) cholesterol, favoring a higher level of LDL compared to HDL cholesterol, which increases the risk for developing cardiovascular disease. Unfortunately, the reduction of Estrogen levels have also been found to impact the reduction of HDL and increase of LDL even more, and so users should be careful when utilizing Masteron so as to ensure their Estrogen levels are not reduced too significantly so as to result in greatly altered HDL:LDL ratios. Supplementation with proper cardiovascular support is highly recommended as well.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737714614564,"sku":null,"price":1180.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c94979e3-2df8-4668-969c-48956ca7cb0a.jpg?v=1778050035"},{"product_id":"keifei-tamoxifen-30-tabs-20mg","title":"Keifei Tamoxifen 30 Tabs 20mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003ePresentation: 20mg per tablet. Orange colour film coated round concave tablet with KF wording imprint on one side. In plastics blister pack of 5 strips x 10 tablets of 50 tablets in a box. Comes with 1 set of 10 digits authentication codes paste on the box.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTamoxifei is commonly referred to in quite a few ways: as a SERM (Selective Estrogen Receptor Modulator), as an anti-estrogen (that is actually incorrect, as we will later see), and finally as a triphenylethylene. I happen to stick with calling Nolvadex a SERM, because out of my three options, it happens to be correct (as we know that calling it an anti-estrogen is incorrect), and pronouncable (as we know that I have no idea how to say \"triphenylethylene\"). Selective estrogen receptor modulators (SERMs) act as either estrogen receptor agonists or antagonists in a tissue-selective manner, lets see what that means to us.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNolvadex actually has quite a few applications for the steroid using athlete. First and foremost, its most common use is for the prevention of gynocomastia. Nolvadex does this by actually competing for the receptor site in breast tissue, and binding to it. Thus, we can safely say that the effect of tamoxifen is through estrogen receptor blockade of breast tissue (1), especially since total body estradiol increases with use of tamoxifen. Clearly, if you are on a cycle which includes steroids which convert to estrogen, you may want to consider nolvadex as a good choice to run along side them.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737775137060,"sku":null,"price":400.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_94fae340-caac-4119-96d4-c61c517570a6.jpg?v=1778050175"},{"product_id":"keifei-sustanon-250-10ml","title":"Keifei Sustanon 250 10ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eChemical Name: Testosterone Propionate, Testosterone Phenylpropionate, Testosterone Isocaproate, Testosterone Decanoate, Mix of Testosterone\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: 250mg\/ml x 10ml multi doses vial and 250ml\/ml x 1ml in single dose ampoule\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePresentation: 10ml multi dose vial x Testosterone Propionate 30mg\/ml, Testosterone Phenylpropionate 60mg\/ml, Testosterone Isocaproate 60mg\/ml, Testosterone Decanoate 100mg\/ml with Keifei® wording imprinted on the side. Seal with grey colour flip off cap with Keifei® wording imprinted. Each vial comes with 1 sets of 10 digits Authentication Code. 10 vials\/ box in white and grey colour outer box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e1ml single dose ampoule x Testosterone Propionate 30mg\/ml, Testosterone Phenylpropionate 60mg\/ml, Testosterone Isocaproate 60mg\/ml, Testosterone Decanoate 100mg\/ml. Each ampoule imprinted with 3 rings on top Red, Green, Red with a red dot below. All wording is imprinted. Pack in 3 ampoules or 10 ampoules of 5 ampoules per tray x 2 in plastics insert with Keifei® imprint on it.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe outer box contains 60 ampoules of 20 inner boxes of 3 Ampoules in white and grey box. Each inner box pack of 3 ampoules comes with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOr the outer box contains 100 ampoules of 10 inner boxes of 10amps in white and grey box. Each inner box pack of 10 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* Remarks: NEW PACKING WITH IMPROVE QUALITY AND QC CHECK UNDER USP STANDARD, KNOW AS KEIFEI® PHARMA.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSustanbolin 250 – It is a mixture of testosterone esters consist of 4 testosterones. Beauty of this drug is designed to provide a fast yet extended release of testosterone. The propionate and Phenyl propionate esters are much faster utilized, releasing into circulation within the 1st 4 days. The other 2 esters are much slower to release and stay in the body for about 2 – 3weeks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSustanbolin is a strong anabolic with pronounced androgenic activity. This is used for bulking cycle. Gains in strength and muscle mass. It does convert to estrogen as it is the nature of testosterone, but it is more tolerable than cypionate and enanthate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBeing a strong testosterone product, all the standard androgenic side effects are also to be expected. Oily Skin, acne, aggressiveness, facial or body hair growth and male pattern baldness are all possible.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53737917284644,"sku":null,"price":540.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d133d339-19f4-42ce-8f04-b6582de92d02.jpg?v=1778050326"},{"product_id":"keifei-growth-hormone-kit-160iu","title":"Keifei Growth Hormone Kit 160iu","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cdiv\u003e\u003cspan\u003eKEIFEI KEFEITROPIN 160iu HGH(140iu somatropin=10x 1ml powder+water)\u003c\/span\u003e\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e191 Amino Acid Chain 99% pure \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: Varies upon injection method\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Growth Hormone\/IGF-1 Precursor (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 2-16 i.u. total daily (1mg=2.7 i.u)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Very rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Very rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Anabolic\/No Androgenic Effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHuman Growth Hormone (GH) has been a subject of debate since I was a kid. Natural (endogenous) GH is produced by the pituitary gland. Children produce 2 i.u. “spurts” 4-7 times per day for 4-5 non-consecutive days during a 2-3 week period (during growth spurts). That would equal 32-70 i.u. in only a 4-5 day span. A healthy adult’s pituitary releases only 0.5-1.5 i.u. daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUntil the mid 1980’s, the only available form of exogenous (occurring outside the body) GH was manufactured by taking the pituitary glands of dead corpses (like there are a lot of “live” corpses running around?) and grinding them up. (I am not joking!). The GH was then extracted and purified through a series of expensive procedures, packed and sold by prescription only for use by children suffering from stunted growth. About 1987, this form of GH was linked to a fatal brain disease called CREUTZFELD-JAKOB DISEASE, and removed from the market.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEnter Genetech and synthetic GH. The first synthetic GH was produced by genetically altering transformed mouse cells \/Ecoli. Natural GH has a 191 amino acid sequence where as the Protropin brand of GH produced by Genetech contains 192 amino acids in its sequence. This may have the affect of causing the body to produce GH anti­bodies which deactivate the GH. Most synthetics now contain the normal 191 amino acid sequence, of which there are over a dozen available today.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH has 3 effects any athlete desires: GH helps the body burn more adipose (fat) tissue by promoting the release of fatty acids to be used as energy. Normally at rest, the body uses about an equal division of fat and carbohydrate calories. When the endocrine system senses a low circulatory level of glucose, the hypothalamus-pituitary-axis (HPA) reacts by releasing GH. The GH then triggers (through a series of enzymic\/chemical reactions) the release of fatty acids from adipose stores so metabolic energy requirements can be met. This means exogenous GH administration has been well documented to do the same.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH has a very potent anabolic (protein synthesis\/tissue building) effect. In exerting anabolic effects, it can cause both hyperplasia (an increase in the number of muscle cells) and muscular hypertrophy (the enlargement of muscle cells). This change in cell number is permanent and therefore means more cells to make bigger. GH also has an anabolic effect on soft tissues such as tendons, cartilage, and other connective tissue. This means old injuries repair and strength increases due to stronger connective tissue… both at an accelerated rate. It is a well known fact that GH is a powerful anti-catabolic agent (protein sparing). This effect has allowed modern bodybuilders to retain or even add significant lean mass tissue during calorie restricted periods (cutting phases) and become the shredded monsters of the new era.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen using GH many athletes were less than satisfied with their results. Most likely this was because they bought bogus GH. It was common to find GH for a hard-core pro bodybuilder cost about $35,000 or more, yearly. To test GH, most simply bought a pregnancy test kit, mix a vial of (hopefully) GH and place a drop or two in the test area. If the test result was “pregnant”..they had been screwed. Most pregnancy test kits test for elevated gonadoltropins (which HCG is and GH is not). For those few, whose bodies manufactured GH anti-bodies (and GH failed to work for you) sorry about your luck. GH, used properly, has overwhelmingly been renowned as a genetic equalizer if used for that purpose.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAny polled athlete chose to use GH as a performance enhancing drug should have first understand at least the basics of its actions.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH itself is not responsible for the majority of the effects seen from GH use. Actually GH is only a precursor to the so-called “good stuff”. When GH passes through the liver, it is converted into INSULIN-LIKE GROWTH FACTORS (such as IGF-1). IGF-1 is a very active but unstable chemical, which is why the body waits until the last second to make it naturally. The liver has a limited capacity to convert excess GH into IGF-1 unless other chemical hormone levels are also elevated. Insulin, T-4\/T-3 thyroid hormones, gonadotropins, androgens\/anabolic hormones, and even estrogen and corticosteroids all play an important role in the positive effects of GH. So they too were often exogenously elevated in what was considered “the correct ratios” by the largest of the self administering athletes. For the liver to convert high levels of GH to IGF-1 several times a day and cause a high quality anabolic response, it was commonly noted that T-3 thyroid hormone and insulin also needed be increased to accomplish the desired effect. Triacana may be strong enough to increase thyroid activity, but Cytomel was considered to be a better choice. Though some seemed to disagree, most emphatically believed that a fast-acting insulin such as HUMULIN-R or Humalog was a better and safer choice of exogenous insulin since they allowed better timing and have a much shorter effective period. This allowed the athletes to time insulin activity with the active period of GH at the optimum absorption times such as upon waking and the first few hours after a work­out. The result was less chance of fat accumulation and a heightened anabolic response. Since GH suppresses natural T-3 thyroid hormone release, the exogenous administration of Triacana or Cytomel allowed for an elevated calorie intake that was utilized more for building muscle and soft tissue than for adipose tissue storage. Many pro bodybuilders used Clenbuterol and\/or ephedrine stacks with GH while dieting. Since Clenbuterol and\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEphedrine both suppress natural insulin release, they usually stacked the GH and Clenbuterol \/Ephedrine with a synthetic T-3 thyroid hormone and sometimes with insulin as well. The use of insulin was dependent upon whether it was a bulking or dieting phase and depending on how their body responded to exogenous insulin use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*I can not stress enough how dangerous insulin use can be. Comas and death are quite possible if used wrong. If you wish to use it, please see a doctor for monitoring.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAAS and\/or Clenbuterol further enhance the anabolic effects of GH. From all but a few polled it was reported that excellent muscle mass gains resulted with the use of GH when other chosen hormone levels were also met (*also see “cycles”) and one could afford it. Also, beware of fake GH. It is more common than you may realize. It is an illegal drug and the black market is not always honest.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe question of dosage was a big one. For the purpose of stunted growth manufacturers of GH (due to pituitary hyophysially caused stunted growth) state 0.3 i.u. weekly per LB of body weight. So for a 235 LB bodybuilder that would equal 70.5 i.u. weekly, meaning a daily total of about 10-i.u. However, even 2-3i.u. daily did produce some nice results over a 6-8 week period when the other reported hormone requirements were met as well. Short high dosage burst cycles too were noted to create these results (which will be discussed later) by the more elite of those polled.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*GH is medically administered intramuscularly or subcutaneously (under the skin). *When multiple injections were utilized, I personally noted better results with subcutaneous administration.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*1-mg=2.7 i.u. of GH and some products are listed as such.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWith exception of those few whose insert states otherwise, the dry unmixed GH substance maybe stored at room temperature. Once the solution has been mixed with the dry GH powder, (SWIRLED, DO NOT SHAKEN) the mixture must be refrigerated and lasts for 24-hours before it begins to degrade. An interesting product has become available called DEPO-NUTROPIN that has an active-life of about a month. This would allow for fewer injections and a reduced price. Also, several patents run out this year so many overseas and less expensive GH preparation will soon be available in the U.S. by prescription only.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Though no negative side effects were reported, the available literature does list several serious ones: Kidneys and heart enlargement, high blood pressure, diabetes, thyroid hormone deficiency, and acromegaly. For the most part, they are rare to say the least and usually would be from extreme dosages and lengths of cycles. But like most hormones, you just do not know until it is a fact for you. Kind of scary, huh?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen GH was utilized with an insulin protocol, it was considered important to space injection periods between GH and insulin about an hour. Also if GH was utilized only twice daily, it was reported best to avoid natural high points of GH release such as first thing in the a.m., post-work out, and right before bed. This was if GH was utilized without insulin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHuman Growth Hormone (somatotropin – also referred to as HGH, or HGH) is created by somatotropes in the pituitary gland of the human brain, the primary form consisting of a 191 amino acid chain. Somatotropes make up more than 50% of the pituitary gland and growth hormone is by far the most important hormone produced there. By the age of 60 most people will have approximately 80% less growth hormone in their system than when they were 20. When we are young, HGH is in big part responsible for the proper growth of bones, muscle, and other tissues. As we become adults, HGH is responsible for keeping muscles from wasting away, supports healthy immune system response, regulates aspects of our metabolic function dealing with increased fat metabolism and healthy body composition in later life, and maintains and repairs our skin and other tissues. HGH, or GH in short, is certainly an effective fat burner and anabolic agent, and is a protein secreted by the pituitary. Once secreted, it has the ability to influence various cells in the body to increase in number and size, as well as having the ability to enhance the movement of amino acids through cell membranes- thereby increasing the rate at which the cells can convert those molecules to usable proteins. It also causes cells to preferentially burn fat in lieu of carbohydrates.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003erHGH\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003erHGH is a human growth hormone produced by recombinant DNA technology derived from engineering Escherichia coli (E. coli), and is identical to the natural growth hormone in amino acid sequence and three-dimension structure. It has a molecular with of 22,125 daltons of which 191 amno acid sequence and structure are identical to the dominant form of the human pituitary growth hormone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH has two distinct types of effects:\u003c\/div\u003e\n\u003cdiv\u003eDirect effects are the result of growth hormone binding its receptor on target cells. Fat cells (adipocytes), for example, have growth hormone receptors, and growth hormone stimulates them to break down triglyceride and suppresses their ability to take up and accumulate circulating lipids.\u003c\/div\u003e\n\u003cdiv\u003eIndirect effects are mediated primarily by an insulin-like growth factor-1 (IGF-1), a hormone that is secreted from the liver and other tissues in response to growth hormone. A majority of the growth promoting effects of growth hormone is actually due to IGF-1 acting on its target cells.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects on Growth\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGrowth is a very complex process, and requires the coordinated action of several hormones. The major role of growth hormone in stimulating body growth is to stimulate the liver and other tissues to secrete IGF-1. IGF-1 stimulates proliferation of chondrocytes (cartilage cells), resulting in bone growth. Growth hormone does seem to have a direct effect on bone growth in stimulating differentiation of chondrocytes.\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 also appears to be the key player in muscle growth. It stimulates both the differentiation and proliferation of myoblasts. It also stimulates amino acid uptake and protein synthesis in muscle and other tissues.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMetabolic Effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGrowth hormone has important effects on protein, lipid and carbohydrate metabolism. In some cases, a direct effect of growth hormone has been clearly demonstrated, in others, IGF-1 is thought to be the critical mediator, and some cases it appears that both direct and indirect effects are at play.\u003c\/div\u003e\n\u003cdiv\u003eProtein metabolism: In general, growth hormone stimulates protein anabolism in many tissues. This effect reflects increased amino acid uptake, increased protein synthesis and decreased oxidation of proteins.\u003c\/div\u003e\n\u003cdiv\u003eFat metabolism: Growth hormone enhances the utilization of fat by stimulating triglyceride breakdown and oxidation in adipocytes.\u003c\/div\u003e\n\u003cdiv\u003eCarbohydrate metabolism: Growth hormone is one of a battery of hormones that serves to maintain blood glucose within a normal range. Growth hormone is often said to have anti-insulin activity, because it suppresses the abilities of insulin to stimulate uptake of glucose in peripheral tissues and enhance glucose synthesis in the liver. Somewhat paradoxically, administration of growth hormone stimulates insulin secretion, leading to hyperinsulinemia.\u003c\/div\u003e\n\u003cdiv\u003eHGH has been the supplement of choice for many professional athletes over the years. American football great, Lyle Alzado, claimed that 80% of all professional American football players, including himself, have taken HGH. HGH has amazing age-reversing effects that make it possibly the strongest anabolic substance available. Some of the benefits associated with HGH supplementation include the reversal of common diseases associated with aging, improved brain activity and function, it strengthens connective tissue which reduces the probability of injury, incredible weight loss without any loss in lean mass, reduces wrinkles by rejuvenating the skin, it raises energy levels and brightens mood, promotes muscle growth, improves libido, improves functions of the lungs which increases the level of oxygen in the blood stream, provides immune system support and Thymus function, and probably the most impressive characteristic is, its ability to produce more muscle cells, something no steroid can do.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePRODUCT DETAILS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e191 amino acid chain recombinant growth hormone 10IU per vial\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePositives to taking growth hormone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH does reduce body fat\u2028\u003c\/div\u003e\n\u003cdiv\u003eHGH does increase muscle mass and shape the body\u2028\u003c\/div\u003e\n\u003cdiv\u003eHGH does rejuvenate the body\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your nails grow faster\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your hair grow faster\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your skin softer and nicer\u003c\/div\u003e\n\u003cdiv\u003eNegatives to taking growth hormone \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eProlonged HGH use does mess with your blood sugar (you need to eat more carbs if you get hypoglycemic episodes)\u2028\u003c\/div\u003e\n\u003cdiv\u003eProlonged HGH use can cause a mild carpal tunnel syndrome (which goes away when you stop taking it)\u003c\/div\u003e\n\u003cdiv\u003eHGH can cause mild water retention (which goes away when you stop taking it)\u003c\/div\u003e\n\u003cdiv\u003eHGH and temperatures\u003c\/div\u003e\n\u003cdiv\u003eCicconatropin is lyophilized (freeze dried) Growth hormone and this is how it withstands temperatures:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBefore reconstituted\u2028- if refrigerated between 2 – 8 degrees Celsius it’s good until expiration date.\u003c\/div\u003e\n\u003cdiv\u003eAt room temperature (up to 37 degrees celsius) it’s good for over 30 days.\u003c\/div\u003e\n\u003cdiv\u003eAt up to 45 degrees celsius it’s good for about a week.\u003c\/div\u003e\n\u003cdiv\u003eAfter reconstituted – it has to be refrigerated at all times. It’s good for 20 days with bacteriostatic water and 24 hours with normal water for injection.\u003c\/div\u003e\n\u003cdiv\u003eWater Bacterostatic water is sterile, has a specific pH level and contains a specific amount of benzyl alcohol as a bacteriostatic preservative, is in a specially formulated polyolefin vial to maintain it integrity and sterility, and has no adulterants that may damage\/breakdown what you are reconstituting or cause a deep tissue infection when injected. It’s what you have to use for IM and subcutaneous injections and reconstituting peptides or growth hormone. Normal water for injection will also work as a diluent for your growth and peptides but the injection is much more painful than bacteriostatic water and the active ingredient downgrade in normal water for injection is much faster than bacteriostatic water. Normal water for injection will keep your growth hormone or peptide active for only 24 hours where as bacteriostatic water will only start downgrading after 14 days. Bacteriostatic water is also much less painful to inject than water for injection. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSyringes Get the insulin type syringe with 100 markings on the side. They are very cheap and available in every local pharmacy store. They have the smallest needles. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMixing\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePull 1ml of water into the syringe and inject it into the vial with powder. GH molecules are very fragile – sensitive to heat and rapid movements. You should never shake the vial when mixing. You should not inject the water directly into the powder with force, but rather let it gently slide down the inside of the vial. If it bubbles up, you should put the vial in the refrigerator and leave it there for about 15 minutes. The bubbles will be gone by then. You should then gently turn the vial between your fingers until all of the powder has dissolved (it takes about 3-4 minutes).\u003c\/div\u003e\n\u003cdiv\u003eThe vials are under vacuum, so before you can take the GH out, you need to get rid of the vacuum. You take a fresh syringe, pull air into it and inject the air into the vial (not into liquid, but into air above the liquid). This will get rid of the vacuum. You can then pull out the GH as you need it. 10 markings on the 100-mark syringe = 1 IU.\u003c\/div\u003e\n\u003cdiv\u003eIf you want to take 2IU you will then draw 20 markings on the insulin syringe and 3IU will be 30 markings as in the picture below.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eINJECTIONS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome people pull the entire HGH vial content into the syringe and use the same for 5 injections. Others prefer to use a fresh syringe for every injection (which is smart in my humble opinion).\u003c\/div\u003e\n\u003cdiv\u003eThe favorite spot for HGH injections is subcutaneously, into the stomach fat – pinch some skin between your fingers and insert the needle at a 45-degree angle. Chose a different spot every time. Depending on the spot, you can either feel nothing or you can feel slight pain – you will learn your favorite spots in time. GH can also be injected into any muscle (thigh, shoulder, etc.) – it works the same either way.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH DOSAGE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage depends on the purpose. People generally use 2IU per day for anti-aging purpose and 4IU per day for bodybuilding, weight loss and general fitness. In case of 4IU, people take 2IU in the morning and 2IU in the afternoon. Its best injected into stomach fat (exactly the same way as insulin).\u003c\/div\u003e\n\u003cdiv\u003eEffects are felt about a week into the first cycle (better sleep, skin improvement, etc.). Improved muscle tone is noticed about a month or two after the start (provided you do good workout and proper diet – plenty of proteins). Don’t just settle for any type of protein, because some manufacturers put in all sorts of crap (artificial flavors, sugar, etc. also some manufacturing methods produce low quality protein which is no good.). You want undenatured whey protein isolate created with micro cross flow filtration method and possibly get unflavored and unsweetened kind. I also suggest you take some good multi vitamin\/mineral supplements.\u003c\/div\u003e\n\u003cdiv\u003eThe effects are most noticeable in the initial few cycles so stay on it for as long as you can (3-4 months even).\u003c\/div\u003e\n\u003cdiv\u003eThe only noticeable side effect, which can happen to some people, is the carpal tunnel syndrome (tingling sensation in your palms and fingers. Feeling like your hands fall “asleep” sometimes, especially in the morning when you wake up). If it gets unbearable, people just stop the cycle for a few weeks and then resume when the carpal is gone. If it happens it does so only in initial few cycles when the carpal tunnel (through which nerves are passing to your palms) is too thin and doesn’t have time to adapt to the new rapid growth. Later on the tunnel adapts and in subsequent cycles the carpal is barely felt – if at all.\u003c\/div\u003e\n\u003cdiv\u003eYou can take your growth hormone once a day for example 2IU per day for anti ageing purposes. You can also split your growth and take 2IU three times per day or more for bodybuilding purposes with only one crucial rule that must apply. Not within an hour before you eat and not within two hours after you have eaten. When insulin spikes in your blood because of a meal it will destroy your growth hormone so we do not want growth hormone in the blood together with insulin from a meal.\u003c\/div\u003e\n\u003cdiv\u003e10 x 10.27iu HGH per vial (3,8mg) plus 10 x 1ml bacteriostatic water plus 10 x 1ml insulin syringes.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH is generally used to aid with recovery and it is recommended for use with EVERY cycle. While it is not really a stand alone anabolic product, it most certainly enhances the effect of regular anabolic’s for beyond expectation. It has also been reported that gains achieve from cycles are also for more easily maintained and the anabolic side effects are minimized. Add to this the fact that it’s also an anti-aging product so you look better in every way you possibly can!\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEutropin – Platinum Range:\u003c\/div\u003e\n\u003cdiv\u003eBeside containing high grade HGH, Eutropin contains Glycine which has been scientifically proven to stimulate the pituitary gland to release higher levels of you own, natural HGH. When you add synthetic hormone to your body there is a risk that your body may reduce production of its natural hormone and the addition of the Glycine is an attempt to reduce this phenomenon. (Please read the Product Insert for advice as to how to minimise this effect)\u003c\/div\u003e\n\u003cdiv\u003eEutropin contains additional excipients which buffer the HGH so as to allow a higher degree of effectivity. According to tests, Eutropin is ±12% more effective than most well known, reputable brands.\u003c\/div\u003e\n\u003cdiv\u003eThe bacteriostatic water contains a preservative which slows down microbial growth in the reconstituted HGH thereby extending the life thereof by up to 4 times.\u003c\/div\u003e\n\u003cdiv\u003e3.8mg HGH per vial which is 10.27iu. This takes care of the small amount one can’t draw out of the vial and ensures you get a full 10iu HGH.\u003c\/div\u003e\n\u003cdiv\u003eContains 10 x 1ml insulin syringes to get you going as soon as you get your kit. No need to run around for syringes. You can also purchase more from us.\u003c\/div\u003e\n\u003cdiv\u003eWe all know we can’t get every last drop of liquid out of the vial. We’ve worked out that this is about 0,025ml and by adding an extra 0,27iu of HGH you are ensured of getting a full 10iu out of the vial.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53739165647140,"sku":null,"price":2750.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_45867dc0-5d96-481a-a894-2ff9efdde77b.jpg?v=1778052052"},{"product_id":"keifei-test-prop-100","title":"Keifei Test Prop 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEFEI T PROBOLIN 100(100MG\/ML TESTOSTERONE PROPIONATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-life: 2-3 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug class: Anabolic\/Androgenic steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Male 50-200mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes, severely\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to Testosterone Propionate possessing a brief active-life of 2-3 days, many athletes involved in tested competitions liked the stuff…a lot. Testing is usually based upon testosterone \/Epitestosterone levels. Though most individuals have a much lower ratio, athletes can have natural ratios of up to 6:1. This is considered a negative test for steroids. usually. By injecting Propionate up to 36 hours before competition, plasma Testosterone levels remained elevated while urine concentrations usually fell within the 6:1 levels. Of course IOC testing protocols would detect any plant origin AAS today. But several groups still simply test for the ratio only.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone Propionate is considered a fast acting testosterone due to effects beginning in about 1 day. The drug reportedly has all the benefits of other testosterones (quick strength and muscle mass increases, increased training aggressiveness, fast post-training recovery) but caused a distinctly lower level of water retention. Users noted an improved muscle pump and increased appetite after one to two days of administration. Even with a high rate of aromatization, propionate did not cause gyno as often as other testosterone esters. Users who realize this normally did so due to less frequent injections: Not due to some special quality of the drug. I liked propionate because an increase in IGF-1 was common during liver deactivation. Also because use could be discontinued at the first sign of overt side effects (thus allowing the chemical to no longer be the cause after 2-3 days post-discontinuance).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA high quality muscle gain has been achieved with 50-100mg Testosterone propionate every 1-2 days, 50mg Winstrol Depot every 2nd day, and 20-25mg of Oxandrolone daily. If Parabolan (76mg every other day) was substituted for Winstrol and Proviron is utilized as an anti-estrogen, this became an excellent pre-contest cycle providing superior hardness. Those who had used Primobolan only and no longer made progress at 200-400 mg weekly made consider progress by stacking 200-400mg Primobolan Depot weekly with 50-100mg of Testosterone Propionate every second day. Improved vascularity was common due to increased in red blood cell count as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen who did use testosterones considered propionate to be the superior choice over any other. 25-50mg of Propionate every 5-7 days stacked with any high anabolic such as Anadur, or especially Durabolin caused a dramatic result with less virilizing characteristics. As always, women who are extremely sensitive to androgens reported the use of 1mg Finasteride daily lowered DHT conversion of Propionate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone propionate is a male sexual hormone with pronounced, mainly androgenic action, possessing the biological and therapeutic properties of the natural hormone. In a healthy male organism, androgens are formed by the testes and adrenal cortex. It is normally produced in women in small physiological quantities. In addition to the specific action that determines the sexual characteristics of the individual, it also has a general anabolic action, manifested in enhancement of protein synthesis. Under the effect of testosterone, body weight increases and urea excretion is reduced. High doses suppress the production of hypophyseal gonadotropin, while low doses stimulate it. It has an antitumor effect on mammary gland metastases.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*It should be noted: Propionate also severely suppresses HPTA function and HCG\/Clomid have been considered post administration stables.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53739239014692,"sku":null,"price":480.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_9808c0b8-c60b-48ce-839c-2e1a379925f2.jpg?v=1778052179"},{"product_id":"keifei-turanabol-10mg","title":"Keifei Turanabol 10mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI TURANABOLIN(10MG 4-CHLORODEHYDROMETHYLTESTOSTERONE\/TAB=100TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC N\/A\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 6-8 hours \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/androgenic steroid ORAL\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003estandard: METHYLTESTOSTERONE(ORAL)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 10-50 mg daily Women 10-20 mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne:NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes, 17-alfa alkylated oral\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh anabolic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOral Turinabol is an anabolic steroid developed and made famous by scientists in East Germany years ago. Actually, this is more a steroid of infamy actually, as it was one of the closely held secrets inside the “East German Doping Machine” I am referring to a state sponsored doping program, called “State Plan 14.25” that operated in East Germany for a period of time between the 1960’s and 80’s. It was an aggressive anabolic steroid administration program, designed with one goal in mind: cheating the Olympic drug test. In many cases, the Olympic athletes, both male and female, were unwitting participants, simply told by their trainers and coaches that they were being given “vitamins” Many of these blue vitamins turned out to be Oral Turinabol, a potent and undetectable (at the time) anabolic steroid. As many as 10,000 unsuspecting athletes were given anabolic steroids during the time the program was active. For a more in-depth look at this dramatic historic event, including the trials of several former East German officials for their participation, I recommend you look at the book “Faust’s Gold: Inside the East German Doping Machine”by Steven Ungerleider.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOT, as it is called, is a potent derivative of Dianabol. It is structurally a cross between methandrostenolone and clostebol (4-chlorotestosterone), having the same base structure as Dianabol with the added 4-chloro alteration of clostebol. This makes OT a “kinder, gentler Dianabol” the new steroid displaying a much lower level of androgenic activity in comparison to its more famous counterpart. Its anabolic activity of chlorodehydromethyltestosterone is somewhat lower than that of Dianabol as well, but it does maintain a much more favorable balance of anabolic to androgenic effect overall. This means that at any given level of muscle-building activity, OT will be much less likely to produce the classic androgenic side effects such as oily skin, acne, aggression, and male-pattern hair loss (if genetically prone) than would Dianabol.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe 4-chloro attachment used with this steroid also inhibits its ability to be aromatized. Therefore, OT is not going to present its user with unwanted estrogenic side effects like water retention, increased fat deposition, or gynecomastia. While Dianabol tends to produce puffiness and a little fat retention in its users, which hides muscle definition, the exact opposite effect usually happens with OT. OT tends to promote gain in lean tissue mass, accompanied by an increased look of density, hardness, and definition due to the intensified androgen to estrogen ratio. For bodybuilding purposes, this makes OT a great pre-contest or cutting steroid, not really a bulking agent of choice. Athletes in sports where speed tends to be a primary focus would also find favor in OT, obtaining a strong anabolic benefit without having to carry around any extra water or fat weight.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen this drug was available in Western Europe, the typical daily dosages used by men were in the rage of 20mg to 40mg. Women would get by on less, usually a single 5mg tablet.That is, unless you were an East German female Olympic swimmer, in which case you could have been swallowing as many as 30 tablets per day (we can understand why long-term virilizing side effects were reported over and over again in the “doping trails”). When used in the recommended dosing levels, OT definitely proves itself as a potent lean tissue builder. Again, it will provide less overall muscle bulk than Dianabol, but with its lack of estrogen conversion, the gains obtained with OT, even if smaller in total, are visibly of better quality. Although there is a clear relationship between OT and Dianabol when it comes to molecular structure, ultimately it would be much more appropriate to be comparing the activities of this steroid to those of other mild, non-aromatizing anabolics like stanozolol, oxandrolone or methenolone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTuranabol is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53739324506404,"sku":null,"price":810.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_7d8b87ab-429b-461d-a66b-de79051e3d00.jpg?v=1778052292"},{"product_id":"keifei-anapolan-50mg","title":"Keifei Anapolan 50mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003estrength and cutting stack of Anadrol at 100mg and Winstrol at 50mg is tried and tested amongst many users.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnother common stack is Anadrol and Dianabol with lower dosages of each, with Dianabol extending to 6 weeks and Anadrol stopping at 4 weeks. For this stack cycle, using Anadrol at 50mg daily and Dianabol at 200mg weekly is likely to produce dramatic results very quickly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePerhaps the simplest and guaranteed to see extreme results stack is one consisting of 50mg of Anadrol daily for the first 6 weeks, combined with Test E at 500mg weekly and Deca-Durabolin at 400mg weekly for 12 weeks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe cycle is followed by a two week break then followed up with 3 weeks of PCT (100mg\/day Clomid for 10 days then followed up with 50mg\/day Clomid for another 10 days). This stack will allow rapid gains at the start with Anadrol, while testosterone and Deca kick in as slower acting injectables for the remained of the cycle\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53739412914468,"sku":null,"price":580.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_ee9fc572-7497-4e03-b094-2bb7d51f5faa.jpg?v=1778052432"},{"product_id":"keifei-tren-a-100","title":"Keifei Tren A 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eChemical Name: Trenbolone Acetate\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: 100mg\/ml x 10ml multi doses vial and 100ml\/ml x 1ml single dose ampoule\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePresentation: 10ml multi dose clear vial with Keifei® wording imprinted on the side. 10ml x Trenbolone Acetate 100mg\/ml. Sealed with black flip off cap imprinted with keifei® wording. Each vial comes with 1 sets of 10 digits authentication codes. 10 vials\/ box in a white and black colour outer box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e1ml single dose ampoule x Trenbolone Acetate 100mg\/ml. Each ampoule imprinted with 3 rings on top blue, black, blue with a blue dot below. All wording is imprinted. Pack in 3 ampoules or 10 ampoules of 5 ampoules per tray x 2 in plastics insert with Keifei® imprint on it.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe outer box contains 60 ampoules of 20 inner boxes of 3 Ampoules in white and black box. Each inner box pack of 3 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOr the outer box contains 100 ampoules of 10 inner boxes of 10amps in white and black box. Each inner box pack of 10 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* Remarks: NEW PACKING WITH IMPROVE QUALITY AND QC CHECK UNDER USP STANDARD, KNOW AS KEIFEI® PHARMA.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eParabolin – A100 Parabolin A100 is a fast-acting trenbolone injectable steroid with a great effect on protein metabolism. Trenbolone is one of the best effective anabolic compounds, promoting protein synthesis, as well as creating a positive nitrogen balance. It is an appetite stimulant and improves the conversion of proteins. In laboratory tests, it has been demonstrated that trenbolone increases protein and decreases fat deposition. It has proven to be an excellent product for promoting size and strength in the presence of adequate protein and calories, promotes body tissue building processes, and can reverse catabolism.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to the characteristics of trenbolone does not convert to estrogen, side effect related to estrogen is not a concern. Other side effects during the cycle are oily skin, aggressive behavior, and acne and hair loss. Do watch out of your kidney and liver when high dosages have been used!\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53739548639524,"sku":null,"price":800.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_518b55e7-202d-456a-838a-251cc3673bc2.jpg?v=1778052606"},{"product_id":"keifei-equipoise-250","title":"Keifei Equipoise 250","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI EQUIBOLIN 250(250MG\/ML BOLDENONE UNDECYLENATE =10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 50\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 7-9 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic \/Androgenic steroid (for injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 150-500mg weekly Women 50-150mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: About 50% less than testosterone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted comments: High anabolic\/moderate androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Moderately (Dose dependent)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone is available as a veterinary steroid under various trade names and was commonly refereed to as EQ by athletes polled. However, the quality is normally quite high due to its use in million dollar race horses. Boldenone was reported as one of the safest and most effective anabolic \/ androgenic injectable steroids used by both power lifters and bodybuilders. This drug brought slow but continuous muscle mass and strength gains over a prolonged period. Gains were mostly of a high quality lean mass nature and were maintained for several weeks after use was discontinued. Improved pumps and vascularity were normal are common attributes while low aromatization brought an improved hardness to users musculature.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales normally reported a dosage range of 150-500mg weekly total, usually utilizing an every other day (EOD) injection schedule. Women made excellent progress with dosages of 50-150mg total weekly with a 1-2 injections weekly schedule. In this dose range, women seldom reported virilizing side effects. Most experienced an elevate libido (cool) with few other negative side effects reported. But in some cases, increased hair growth on face and legs were noted. This was usually due to higher dosages however and predominantly limited to existing hair (not new hair growth).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to Boldenone’s reported “non-toxic to the liver” structure, most users experienced great gains with none or few negative side effects. The appetite and red blood cell production stimulating effects of Equipoise marked this drug as a standard for those who sought few negative side effects with quality muscle mass gains. Obviously with increased red blood cell count an increase in oxygen transport was also realized, as was improved nutrient transport.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to a double carbon bond between carbons one and two, boldenone experiences only slight DHT conversion by the 5-alfa-reductase enzyme and is fairly resistant to aromatization to estrogens.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMale athletes commonly stacked Boldenone with testosterone and\/or Anadrol-50 for mass and strength cycles. Pre-contest cycles utilizing this drug often included Trenbolones, Winstrol, and anti-estrogens to create the ultra hard and vascular look.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Personal experiences with Boldenone have resulted in very high quality lean tissue and freaky vascularity. This quite beneficial from a competitive appearance stand-point but long term use resulted in an unfavorable CBC result. I believe my error was in protocol length.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone (1,4-androstadiene-3-one-17β-ol, available as the undecylenate ester)is an anabolic steroid developed for veterinary use, mostly for treatment of horses. It is not indicated for use in humans in the US and is only available through veterinary clinics.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe activity of boldenone is mainly anabolic, with a low androgenic potency. It has a very long half-life, with minimal blood levels present up to 8 weeks after discontinued use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys. The drug is commonly used in doping within bodybuilding. If intended to assist in bodybuilding, the drug is taken as part of a steroid stack of other anabolic steroids, usually with a potent androgen like testosterone as the ‘base’ of the stack.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone has a low rate of aromatization (about 50% of Testosterone), which means it does not convert to estrogen easily and does not cause very much water retention. Many Bodybuilders will find that it is a good replacement drug for Nandrolone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is a poor drug of choice for any athlete who will be subject to a blood test due to its long metabolic half-life. Trace amounts of the drug can easily be detected for months after discontinued use.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53739857805604,"sku":null,"price":720.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_8db5f835-45bc-44cc-8563-6c06743a9686.jpg?v=1778053033"},{"product_id":"keifei-npp-100","title":"Keifei NPP 100","description":"\u003cp\u003e\u003cspan\u003eChemical Name: Nandrolone Phenylpropionate\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: 100mg\/ml x 10ml multi doses vial and 100mg\/ml x 1 single dose ampoule\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePresentation : 10ml multi dose clear vial with Keifei® wording imprinted on the side. 10ml x Nandrolone Phenylpropionate 100mg\/ml. Sealed with purple flip off cap imprinted with keifei® wording. Each vial comes with 1 sets of 10 digits authentication codes. 10 vials\/ box in a white and purple colour outer box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e1ml single dose ampoule x Nandrolone Phenylpropionate 100mg\/ml. Each ampoule imprinted with 3 rings on top brown, white, brown with a brown dot below. All wording is imprinted. Pack in 3 ampoules or 10 ampoules of 5 ampoules per tray x 2 in plastics insert with Keifei® imprint on it.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe outer box contains 60ampoules of 20 inner boxes of 3 Ampoules in a white and purple box. Each inner box pack of 3 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOr the outer box contains 100 ampoules of 10 inner boxes of 10amps in white and purple box. Each inner box pack of 10 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* Remarks: NEW PACKING WITH IMPROVE QUALITY AND QC CHECK UNDER USP STANDARD, KNOW AS KEIFEI® PHARMA.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecaphenylbol -This ester said to be a fast release and long acting compound. Will break down to more potent metabolite in androgen target tissue. There for it is far less likely to cause unwanted androgenic side effect. Basic androgenic side effects are oily skin, acne, body or facial hair growth, aggression and accelerated hair loss.Side effect are mild due to liver can convert Nandrolone to estradiol. But there are still some strong occurrences oily skins, acne, body or facial hair growth, and hair loss are very rare.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740127748388,"sku":null,"price":570.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_60a7aaea-5ff1-44e5-965f-0302086547eb.jpg?v=1778053407"},{"product_id":"keifei-lovers-peptide-pt141","title":"Keifei Lover's Peptide - PT141","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI PT141(10MG\/2ML VIAL) \n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePT-141 or Bremelanotide is the generic term for a research peptide being studied for its possible use in helping to improve sexual dysfunction in both men (erectile dysfunction or impotence) and women (sexual arousal disorder). PT-141 was developed from the tanning peptide Melanotan 2, which is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis that is known as alpha-Melanocyte stimulating hormone. MSH, activates certain melanocortin receptors in the process of exerting its effects. Indeed, MSH also exerts potent influence over lipid metabolism, appetite, and sexual libido. Resultantly, PT-141 has been shown in studies to exhibit libido-enhancing effects by activating the melanocortin receptors MC1R and MC4R, but not skin tanning. Melanotan 1 and Melanotan 2 have been researched for their use in protecting against the harmful effects of ultraviolet radiation from sunlight due to their melanogenesis-stimulating properties.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePT-141 is a potential remedy for the treatment of sexual dysfunction; specifically, male erectile dysfunction. Studies have shown that PT-141 does not act on the vascular system like former compounds, but allegedly works by activating melanocortin receptors in the brain, therefore helping increase ones sexual stimulation. PT-141 is a melanocortin based peptide that has shown effectiveness in clinical studies on both male and female rats. Male rats have shown erectile response with doses as low as 1-2 mgs whereas most female rats have shown positive results with higher doses around 2-3 mgs. While the dosage requirements tend to be higher for female rats, the observable results in female rats tend to be stronger.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740192235812,"sku":null,"price":580.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_565082e5-5cb3-4d6c-98c7-5064d63e0351.jpg?v=1778053527"},{"product_id":"keifei-tren-e-100","title":"Keifei Tren E 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eChemical Name: Trenbolone Enanthate\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: 100mg\/ml x 10ml multidoses\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePresentation : 10ml Multidoses clear vial with keifei® wording imprinted on the left. 10ml x 100mg Trenbolone Enanthate. Sealed with dark purple flip off cap imprinted with keifei®. Each vial come with 1 set of 10digits Authentication codes. 10 vials\/ box in a white and dark purple colour outer box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* Remarks: NEW PACKING WITH IMPROVE QUALITY AND QC CHECK UNDER USP STANDARD, KNOW AS KEIFEI® PHARMA.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eParabolin – E100 This trenbolone enanthate ester is create to replace the hexahydrobenzylcarbonate ester. Trenbolone Enanthate is both unique and incredibly obvious at the same time. On the other hand, attaching an enanthate ester o trenbolone seem like a simple idea at best. After all, we are all familiar with testosterone and methenolone enanthate. This is much lower releasing drug, and offers a great alternative to frequent injections of trenbolone acetate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe base of trenbolone is well understood that it is non aromatizable compound, estrogenic side effects are not expected. Trenbolone alone should not caused any side effects like water retention and gynecomastia but it may intensify the estrogenic traits of other steroids. effects during the cycle are oily skin, aggressive behavior, and acne and hair loss. Do watch out of your kidney and liver when high dosages have been used.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740284838180,"sku":null,"price":800.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d7ab25d9-edd2-4d2b-9790-d0b9a2d76321.jpg?v=1778053656"},{"product_id":"keifei-deca-blend-300","title":"Keifei Deca Blend 300","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI NANDROBOLIN BLEND 300(300MG\/ML NANDROLONE BLEND=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 37\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 125\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 14-16 days for NANDROLONE DECOANATE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (For Injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: Men 200-600mg weekly Women 50-100mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes, in higher dosages in androgen sensitive individuals\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Some, much less than testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare (When used in dosages over 600-mg weekly)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Low, converts to less active norestrogens\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: None.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: No, converts to NOR- DHT with low activity\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: Highly anabolic\/moderate androgenic effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone Decanoate is a very anabolic, moderate androgenic form of nortestosterone that was the most commonly used drug to create a rapid build-up of lean muscle mass or as a diet “protein- sparing” drug by athletes of all kinds. This is a longer lasting nandrolone than Durabolin so some water retention resulted with long term administration (especially in higher dosages). A prominent positive nitrogen balance occurs with the use of nandrolones and therefore a high protein intake was a must for all reported users. If you read the section on protein, you know that nitrogen in its bonded form is a part of protein\/amino acids. Since nandrolone promotes nitrogen storage in muscle cells (a positive nitrogen balance) then the cell contains more protein for growth and repair than normal. Remember: This could only happen if above normal calories (with a focus on protein) were ingested. Since nandrolone is moderately androgenic, good strength gains also resulted. Another plus for nandrolone was that most users experienced a joint healing effect during cycles and a suppressed cortisol\/cortisone activity due to nandrolones ability to long-term block cortisol receptors. Since aromatization was low, in 200-400-mg weekly dosages, anti-estrogens were not commonly necessary to avoid gyno and estrogenic induced side effects. Based upon available research and information available it seems liver toxicity is unknown with nandrolone. So it was not a surprise to find that even those with liver disease have used this drug with great success.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCommon dosages for men were 200 600mg weekly. Though dosages over 400 mg weekly caused more water retention. For first time use of dosages over 400 mg weekly, I preferred to add 50-100mg Durabolin to each of the 2 weekly injections. This was because Durabolin is much faster acting and therefore creates chance for water retention and gyno. (This applied to first -time users only)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAn added benefit of this method was that nandrolone decanoate begins significant activity at 6 days and peaks at about 8 days after administration. The faster acting durabolin “kicks in” after about 1 day. This also resulted in higher “quality” muscle tissue gain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen seemed to do very well with nandrolones due to the lower androgenic\/masculining effect. Women consistently reported excellent lean mass and strength gains at dosages of 50-100 mg weekly. Masculine effects usually were avoided by single weekly injections of 25-50 mg nandrolone decanoate and 25-50 mg of Durabolin (nandrolone phenylpropionate). In both men and women, this method seemed to result in more “quality” muscle, less water retention, less gyno for males, and good retention of gains after the cycle ends.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Metabolites can be found in urine or blood tests for 12-18 months after use of nandrolone is discontinued.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNOTED POSITIVE EFFECTS OF NORTESTOSTERONE (NANDROLONE)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Significant anabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*High quality (but slow) lean tissue gains.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Excellent post-cycle lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Low-moderate water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Low aromatization to estrogens.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Does not negatively effect HDL.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Moderate strength and weight gain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Noted improvement in joint\/soft tissue function.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Excellent protein sparing \/anti-catabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Inhibition of fat synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased metabolic rate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Does not reduce to DHT (Dihydrotestosterone)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Very low-moderate HPTA function inhibition. (Dose Dependent)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased muscle glycogen synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased Creatine Phosphate (CP) synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Reduction in total triglyceride and cholesterol levels.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Beneficial\/improved insulin metabolism.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePOSSIBLE NEGATIVE EFFECTS OF NORTESTOSTERONE (NANDROLONE)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Poor protection from over training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Some males experienced decreased libido (Not true for women) *Inhibition of HPTA function at dosages in excess of 400 MG weekly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone binds to the androgen receptor to a greater degree than testosterone, but due to its inability to act on the muscle in ways unmediated by the receptor, has less overall effect on muscle growth. The drug is also unusual in that unlike most anabolic steroids, it is not broken down into the more reactive DHT by the enzyme 5a-reductase, but rather into a less effective product. As such, some of the negative effects associated with most such drugs are somewhat mitigated.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe positive effects of the drug include muscle growth, appetite stimulation and increased red blood cell production and bone density. Clinical studies have shown it to be effective in treating anaemia, osteoporosis and some forms of neoplasia including breast cancer, and also acts as a progestin-based contraceptive. Nandrolone is also extensively used by bodybuilders and other athletes seeking an edge in professional competition\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740387828004,"sku":null,"price":830.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_15935ecb-6485-42b7-a4c5-1242c233821a.jpg?v=1778053813"},{"product_id":"keifei-igf-1-lr3","title":"Keifei IGF-1 LR3","description":"\u003cdiv\u003e\u003cspan\u003eKEIFEI IGF-1 LONG R3(100MCG SOMATOMEDIN C\/VAIL=3 POWDER+WATER) \u003c\/span\u003e\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life:10 min FOR IGF-1 to 20-30 hours for IGF-1 Long R3\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Growth Factor\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 60-1000mcg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Diet dependent\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF1 LR3 allows for many of the growth-promoting effects of growth hormone insulin-like growth factors also know as IGF’s. IGF-1 LR3 comprises a family of peptides (protiens) that play important roles in mammalian growth and development. IGF1 LR3 is also known as Long R3 IGF-1 or Insulin-Like Growth Factor-I Long Arg3.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe Long R3 IGF-1 version is significantly more potent than regular IGF-1. The enhanced potency is due to the decreased binding of IGF1 LR3 to all known IGF binding proteins. These binding proteins normally inhibit the biological actions of IGF’s therefore IG-1 LR3 has been shown to have increased efficacy and function . \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis IGF-1 LR3 analog of IGF-1 has been created with the purpose of increasing the biological activity of the IGF peptide. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF1 LR3 is also known as Long R3 IGF-1 or Insulin-Like Growth Factor-I Long Arg3. This is a human recombinant, single, non-glycosylated, polypeptide chain containing 83 amino acids and having a molecular mass of 9200 Daltons. IGF1 mediates many of the growth-promoting effects of growth hormone (GH; MIM 139250). The LR3 is a long-term analog of human IGF-1, specifically designed and manufactured for mammalian cell culture to support large-scale manufacturing of recombinant biopharmaceuticals. Early studies showed that growth hormone did not directly stimulate the incorporation of sulfate into cartilage, but rather acted through a serum factor, termed ‘sulfation factor,’ which later became known as ‘somatomedin’.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 LR3 is the primary protein involved in responses of cells to growth hormone (GH): that is, IGF-I is produced in response to GH and then induces cellular activities. One such example is muscle growth or hyperplasia. This compound also makes the human body more sensitive to insulin. It is the most potent growth factor found in the human body. IGF-1 causes muscle cell hyperplasia, which is an actual splitting and forming of new muscle cells.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe most effective form of IGF-1 is considered to be IGF-1 LR3. This formula has been chemically altered to avoid binding to proteins in the human body, and to increase the half life, approximately 20-30 hours.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 is naturally produced in the liver as a result of GH (Growth Hormone) metabolism in the presence of insulin. Muscle tissue can also produce IGF-1 by way of an intracellular response. In fact, one of the benefits of training sets that result in an intense burn, or stretch position training, is the production of natural IGF-1. It is also a side effect of oral 17-ALFA ALKYLATED STEROIDS, which cause a higher release of IGF-1 from the liver. IGF-1 receptors exist throughout muscles and organs such as the heart, spleen, small intestines, and kidneys with a higher concentration of receptors exerting effects upon organs. IGF-1 is extremely anabolic, far more so than GH or Insulin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eRecombinant IGF-1 (genetically engineered) was reported to be effective when injected intramuscularly because it causes localized growth. This was the most popular method, and the agreed wisest for the most part. The drug has a half-life of about 10 minutes, and if it is or has been bound to IGF -BP-3, (INSULIN GROWTH FACTOR BINDING PROTEIN)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ethe half- life is extended to about 12 hours. Pro’s often stacked Insulin and\/or GH with IGF-1 because IGF-1 shuts off natural GH production and GH causes Insulin resistance. IGF-1 is often referred to as Pro-insulin because it counteracts Insulin resistance and interacts with insulin. But this would actually be an untrue term for\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 can have all the side effect of GH or insulin use with an added negative: gastrointestinal (GI) growth. This is due to a higher number of IGF-1 receptors being located in the GI tract as compared to skeletal muscle. The latter has more GH receptors. This explains much of the bloat seen in pro bodybuilders of late.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 is not stable in synthetic forms. A loud noise, shaking a vial, and sudden heat changes can render it nothing more than a bunch of expensive amino acids. Picture a piece of string folded up in a specific shape and held in that shape by a few fibers. This is what an amino acid sequence for GH or IGF-1 looks like, but the IGF-1 sequence has only 2 fibers keeping the active shape. The strand or string is a specific amino acid sequence. The shaping fibers holding the active shape are called disulfide bridges. Change the folding or break a bridge and the IGF-1 no longer fits into its receptor-site. Like a key must have a specific shape to actuate its lock, so must a drug have the right shape to actuate its receptor. Again, this explains the common noted necessity of careful preparation and site-specific injection (into the muscle group trained that day) when IGF-1 was administered.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCommon stacks have been 0.25-0.50-mg of GH per KG of body weight stacked with 60-1000mcg of IGF-1 divided into 2-5 daily injections. Many had reported improved lean mass gains by combining both with insulin and high androgen AAS (Such as testosterone or orals such as DIANABOL and \/or ANADROL-50) for 4-8 weeks. Many simply injected 40-mcg of IGF-1 directly into the muscle group trained that day after training. It is important to note that IGF-1 can cause hypoglycemia and blood sugar monitoring was considered paramount by most.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*The reader should note that IGF-1 has been used clinically on children at dosages of over 3-7mg daily. That is 3,000-7,000 mcg a day! No negative side effects were recorded, though none were expected… of course. The point being is that the 40-100 mcg of IGF-1 used by athletes is most likely insufficient, yet very expensive. However, the results some individuals have realized through IGF-1 use are amazing.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eI have personally noted amazing new growth as a result of past IGF-1 administration. However it is important that readers realize that long term negative side effects have not been well studied. Anything that possesses genetic altering potential has equally negative potential as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eInsulin-like growth factor (IGF-1: originally called somatomedin) has been known to be produced by live under the influence of human growth hormone (HGH). The mature systemic type of IGF-1 is a simple 70 amino acid peptide, but its gene is unexpectedly large spanning a region of over 90 kb of genomic DNA. Alternative splicing of IGF-1 gene results in different transcripts encoding several IGF-1 precursor proteins. IGF-1 has been shown to be involved in several cellular processes including tissue differentiation,maintenance of tissue mass and tissue repair . And it is known to be mitogenic and myogenic. IGF-1 is thought to be responsible for much of the anabolic activity of HGH, including nitrogen retention and protein synthesis as well as causing muscle cell hyperplasia (increase in number of muscle cells), and mitogenesis (the growth of new muscle fibers). In fact, IGF-1 acts on several different tissues (not just muscle) to enhance growth through various mechanisms. The easiest way to think about IGF is that it is a primary factor in the anabolic effects of weight training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 Long R3\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMany IGF-1 variations have been developed for research and bodybuilding use. IGF-1 Long R3 (or Long R3 IGF-1) is the most effective form of IGF-1. it has been chemically altered and has had amino acid changes which cause it to avoid binding to proteins in the human body and allow it to have a much longer half life, around 20-30 hours. Long R3 IGF-1 is an 83 amino acid analog of IGF-1 comprising the complete human IGF-1 sequence with the substition of an Arg(R) for the Glu(E) at position three, hence R3, and a 13 amino acid extension peptide at the N terminus. This analog of IGF-1 has been produced with the purpose of increasing the biological activity of the IGF peptide. All these alterations make IGF-1 Long R3 significantly more potent (2-3x) than IGF-1 in studies, because it has a lower affinity to be rendered inactive by IGF binding proteins. Yeah, all effects of IGF-1 still holds true for this version, but it?s just a bit more active in the body, and hence more potent. It is also not as expensive since a media grade version is available which is sufficient for bodybuilding use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eExperiments have been carried out using the cDNA of IGF-1(a compound which was responsible for directing over expression of IGF-1) in an adenoviral vector under the control of a muscle regulatory sequence. Results were shown by Fig.1. It was found that a single intramuscular injection of IGF-1 cDNA into a mouse muscle resulted in a 15% increase in mean muscle fibre cross section area and a 14% increase in strength in young adult mice within four months. It was concluded due to the anabolic effect of IGF-1. But those effects are not all that the researchers have found. IGF also seems to prevent aging-related muscle changes in old adult mice. These old mice experienced a 27% increase in strength as compared with uninjected old muscles. Muscle mass and fiber type distributions were maintained at levels similar to those in young adults. The researchers have speculated that these effects are primarily due to stimulation of muscle regeneration via the activation of satellite cells by IGF-I \u003c\/div\u003e\n\u003cdiv\u003eBut how effective does IGF-1 Long R3 work on bodybuilders? It’s difficult to put a number on results, since they’re so subjective, but as a general rule, experienced users have found IGF-1 Long R3 to add up to 5% to their lifts in a cycle alone, and a decent reduction in body fat coupled with an increase in muscle gain. A five to ten pound sway each way is possible. The less experienced you are with chemical enhancement, typically the greater the results you can achieve with IGF-1 Long R3 (or any body enhancement chemical). In addition, users report a steady decrease in bodyfat percentage levels due to increase in muscle tissue. Users and researchers have reported most effective results with a 6 weeks on and 4 weeks off cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMechanism\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow does IGF-1 work? To understand how IGF-1 works we have to understand how muscles grow. The ability of muscle tissue to constantly regenerate in response to activity makes it unique. It’s ability to respond to physical\/mechanical stimuli depends greatly on satellite cells. Satellite cells are muscle precursor cells which also might be thought of as “pro-muscle” cells. They are cells that reside on and around muscle cells. These cells sit dormant until called upon by growth factors such as IGF-1. Once this happens these cells divide and genetically change into cells that have nuclei identical to those of muscle cells. These new satellite cells with muscle nuclei are critical if not mandatory to muscle growth. Whenever a muscle grows in response to functional overload there is a positive correlation between the increase in the number of myonuclei and the increase in fiber cross sectional area (CSA). When satellite cells are prohibited from donating new nuclei, overloaded muscle will not grow [10, 11]. So one important key to unnatural muscle growth is the activation of satellite cells by growth factors such as IGF-1.\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 stimulates both proliferation (an increase in cell number) and differentiation (a conversion to muscle specific nuclei) in an autocrine-paracrine manner, although it induces differentiation to a much greater degree. This is in agreement with the Dual Effector theory. In fact, you can inject a muscle with IGF-1 and it will grow. Studies have shown that , when injected locally, IGF-1 increases satellite cell activity, muscle DNA content, muscle protein content, muscle weight and muscle cross sectional area. \u003c\/div\u003e\n\u003cdiv\u003eScientists are now discovering the signaling pathway by which mechanical stimulation and IGF-1 activity leads to all of the above changes in satellite cells, muscle DNA content, muscle protein content, muscle weight and muscle cross sectional area just outlined above. This research is stemming from studies done to explain cardiac hypertrophy. It involves a muscle enzyme called calcineurin which is a phosphatase enzyme activated by high intracellular calcium ion concentrations. Note that overloaded muscle is characterized by chronically elevated intracellular calcium ion concentrations. Other recent research has demonstrated that IGF-1 increases intracellular calcium ion concentrations leading to the activation of the signaling pathway, and subsequent muscle fiber hypertrophy . In summary the researchers involved in these studies have explained it this way, IGF-1 as well as activated calcineurin, induces expression of the transcription factor GATA-2, which accumulates in a subset of myocyte nuclei, where it associates with calcineurin and a specific dephosphorylated isoform of the transcription factor nuclear factor of activated T cells or NF-ATc1. Thus, IGF-1 induces calcineurin-mediated signaling and activation of GATA-2, a marker of skeletal muscle hypertrophy, which cooperates with selected NF-ATc isoforms to activate gene expression programs leading to increased contractile protein synthesis and muscle hypertrophy.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage and Administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe magic effects happens between 60mcgs and 120mcgs per day, in divided doses. In general, people who have used less, and even up to 50mcg\/day have had mediocre results. People who have used more have suffered headaches and nausea, and generally not much more in the way of results.\u003c\/div\u003e\n\u003cdiv\u003eIt has been clearly observed in studies that when GH and IGF-1 are used together, you’ll get greater results in the accumulation of Lean Body Mass than you would by using either of them alone[15]. In addition, there is a very strong probability that testosterone would be synergistic to GH[16], and would also increase IGF levels in muscle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDifferences between IGF-1 and HGH\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH is actually closely related to IGF-1, in a lot of ways. HGH, or GH in short, is certainly an effective fat burner and anabolic agent, and is a protein secreted by the pituitary. Once secreted, it has the ability to influence various cells in the body to increase in number and size, as well as having the ability to enhance the movement of amino acids through cell membranes- thereby increasing the rate at which the cells can convert those molecules to usable proteins. It also causes cells to preferentially burn fat in lieu of carbohydrates. The important thing to realize is that there is a mounting body of evidence that strongly suggests that these effects occur as a result of the IGF-1 released as a result of the pituitaries GH secretion. Scientists have discovered that many of HGH’s anabolic and regenerative effects are actually mediated by IGF-1. HGH indirectly causes muscle growth by stimulating the release of IGF-1 when it (the HGH) is destroyed in the human body. So one way you could look at it as HGH being a precursor to IGF-1. The later is more effective at directly causing muscle growth and density increases than HGH. Over the past few decades, HGH has developed quite a reputation for taking awhile (often several weeks) for the user to start seeing results. In contrast, IGF-1 often begins to product noticeable results within the first couple of weeks. With growth hormone you need to use high amounts of anabolics and often insulin to see any gains at all, this is not the case with IGF-1. IGF-1’s superiority to HGH is not only intuitive at some level, but has also been clearly elucidated clinically as well. In the following graphs taken from a rodent study comparing IGF-1 and HGH, a low dose as well as a high dose of IGF-1 was shown to be more anabolic than HGH. In comparison to HGH, IGF-1 produced an overall greater total protein content within the injected muscle as well as a greater final weight of the that muscle (called the “Tibialis Anterior” or TA)\u003c\/div\u003e\n\u003cdiv\u003eIt seems to be the case that IGF-1 would be superior to HGH as an anabolic agent. In some clinical studies, that is not always the case, but in most of bodybuilders and athletes, greater results are often seen with IGF-1 over HGH – and it should be noted that they are often seen more quickly as w\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740488458532,"sku":null,"price":850.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_f83441aa-f8d0-408f-902b-39e5fc4d6c58.jpg?v=1778053923"},{"product_id":"keifei-aromasin-30-tabs-25mg","title":"Keifei Aromasin 30 Tabs 25mg","description":"\u003cp\u003e\u003cspan\u003eDosage: 25MG every 3rd day or it can be split to 12.5MG for two days on ,one day off.\u003c\/span\u003e\u003cspan\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003eChemical Name: Exemestane\u003c\/div\u003e\n\u003cdiv\u003eQuantity: 30 tabs\u003c\/div\u003e\n\u003cdiv\u003ePicture may differ from actual product\u003c\/div\u003e\n\u003cdiv\u003eCategories: All Anti Estrogen, All Products, Keifei Pharma, Keifei Pharma Anti Estrogen\u003c\/div\u003e\n\u003cdiv\u003eTags: Aromasin, Buy Keifei, Exemestane, Exemestic, Keifei Anabolics, Keifei SA\u003c\/div\u003e\n\u003cdiv\u003eBrand: Keifei Pharma\u003c\/div\u003e\n\u003cdiv\u003eDescription\u003c\/div\u003e\n\u003cdiv\u003eUsers can expect to see a dramatically lower level of estrogen in the body when using Aromasin. The reason for this is due to it blocking the aromatase enzyme. This is the enzyme in the body responsible for converting testosterone into estrogen. Aromasin and Testosterone, Aromasin blocks the aromatase enzyme, which is responsible for converting testosterone into estrogen. When this happens, there is a dramatic decrease of testosterone in the body. Since many bodybuilders want to be at low levels of estrogen, they will stop taking Aromasin. This can lead to a rebound in estrogen levels and potentially increased oils and water retention Aromasin does not affect DHT levels in the body, which might be a concern for some users. However, Aromasin is not an anti-androgen. It only has a mild effect on DHT levels when used in combination with testosterone.\u003c\/div\u003e\n\u003cdiv\u003eUsers can also expect to see a significant decrease in estrogenic side effects such as gynecomastia due to this. Aromasin, which is one of the first AAS to be marketed, also improves natural production of testosterone. This drug is generally prescribed as a last resort and when other treatments fail to produce desired effects.\u003c\/div\u003e\n\u003cdiv\u003eUsers should not expect to see prevention of side effects caused by DHT based steroids as these do not convert to estrogen. The only proven way to prevent the side effects caused by DHT is a drug called Finasteride. Finasteride helps prevent the side effects that may be caused by 3-alpha-reductase (DHT) in men who are predisposed to those side effects, such as baldness and prostate enlargement. Bodybuilders can also expect to see a decrease in libido, which is caused by the conversion of testosterone to DHT.\u003c\/div\u003e\n\u003cdiv\u003eAnabolic Androgenic Steroids and Testosterone Anabolic androgenic steroids are synthetic derivatives of testosterone that are used primarily in medicine to treat certain diseases, but also used as performance-enhancing drugs. For example, Anadrol 50 is an anabolic androgenic steroid that is prescribed to treat androgen deficiency.\u003c\/div\u003e\n\u003cdiv\u003eTestosterone is the primary male sex hormone, responsible for the development of male secondary characteristics during fetal development. Testosterone production in males begins at approximately week 4 of gestation, with maximal levels reached by 9 to 12 weeks. The testes contain the majority of testosterone produced in males, with smaller amounts produced by the adrenal glands and rest of the body. It is the presence of testosterone that causes certain physical changes associated with puberty in males. Manufactured versions of testosterone preparations may be obtained as a prescription drug. There are also many hormone preparations available without a prescription.\u003c\/div\u003e\n\u003cdiv\u003eAromasin is a powerful aromatase inhibitor which is what makes it also valued so highly by people who use anabolic steroids.\u003c\/div\u003e\n\u003cdiv\u003eThe main use you’ll be having for Aromasin is to use it on a steroid cycle to stop estrogen related side effects with the most important one being gynecomastia (gyno).\u003c\/div\u003e\n\u003cdiv\u003eExemestic, which is the active compound and chemical name of Aromasin, works by blocking the effects of estrogen in the breast tissue so the growth of cancer can be limited or stopped.This breast tissue targeted estrogen blocking action of this aromatase inhibitor is useful for bodybuilders who use anabolic steroids with aromatizing effects which cause estrogenic side effects – specifically gynecomastia (gyno), or male breast tissue enlargement.\u003c\/div\u003e\n\u003cdiv\u003eWhen we let gyno take hold while using steroids, the effects are not only ugly and embarrassing to look at, but they can be impossible to get rid of without surgery. So, making use of an aromatase inhibitor like Aromasin is one of the most important things a male steroid user must do.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEFFECTS ON CYCLE:\u003c\/div\u003e\n\u003cdiv\u003eAromasin For Gynecomastia and Estrogen Control\u003c\/div\u003e\n\u003cdiv\u003eAromatase inhibitors including Aromasin have become a vital tool for steroid users in the battle to combat estrogen related side effects during a steroid cycle.\u003c\/div\u003e\n\u003cdiv\u003eOne of most feared estrogenic side effects from steroids which aromatize is gynecomastia – male breast tissue enlargement. If not adequately controlled, then this condition can become irreversible through any means besides invasive surgery.\u003c\/div\u003e\n\u003cdiv\u003eAdditional estrogen related side effects we need to control with an aromatase inhibitor include water retention and the high blood pressure that can come with allowing water retention to reach a high level.\u003c\/div\u003e\n\u003cdiv\u003eAIs like Aromasin work more universally than another type of drug that’s popular with steroid users; SERMs which are selective in the tissue they target. Aromasin on the other hand can lower overall serum estrogen levels by blocking the process of aromatization. When the steroids you’re using convert testosterone to estrogen, this is an aromatizing process and one which most steroids will cause.\u003c\/div\u003e\n\u003cdiv\u003eAromasin is a powerful and effective way to lower your estrogen levels while on a steroid cycle so you can reduce or even completely prevent estrogenic side effects like gyno, and this drug is known to be very effective at lowering estrogen.\u003c\/div\u003e\n\u003cdiv\u003eStudies show that Aromasin can lower estrogen levels and increase testosterone concentrations in males. It was found that the drug works fast to start suppressing estrogen, with concentration of the drug being at its highest level just one hour after a 25mg dosage, and the maximum level of estrogen suppression was seen at the 12-hour mark.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage Instructions\u003c\/div\u003e\n\u003cdiv\u003eRecommended Dose: 25MG every 3rd day or it can be split to 12.5MG for two days on ,one day off.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromasin is a very potent aromatase inhibitor and new users, as well as experienced ones, will find that ongoing adjustments are not only ideal but recommended when it comes to both your dosage and frequency.\u003c\/div\u003e\n\u003cdiv\u003eRather than just copying what someone else is taking so you can get the best outcome of mitigating estrogenic side effects without taking more Aromasin than you need and striking a balance between effective estrogen control and avoiding detrimental side effects.\u003c\/div\u003e\n\u003cdiv\u003eAromasin Dosage During Anabolic Steroid Use\u003c\/div\u003e\n\u003cdiv\u003eLow doses of Aromasin are effective at reducing estrogen levels while on a steroid cycle. This isn’t a drug that needs to be taken every day while you’re on a cycle, and most of the time a two to three days per week is administration does the job.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMost people will find that 12.5mg every two days works very well, but your dose and frequency will heavily depend on the intensity of the steroids you’re using and your individual sensitivity to estrogen and Aromasin itself.\u003c\/div\u003e\n\u003cdiv\u003eIn rare circumstances some guys will find that a 25mg dose every two days or even every day is required to keep estrogen at bay, but due to possible effects on cholesterol this high level of Aromasin intake should only be done for a short period of time as needed.\u003c\/div\u003e\n\u003cdiv\u003eFemale Aromasin Dosage\u003c\/div\u003e\n\u003cdiv\u003eWoman who uses steroids don’t have the same concerns as men when it comes to estrogen levels. Additionally, Aromasin is a very powerful inhibitor of estrogen so young women will not want to reduce estrogen levels to the extent that this drug is able to.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome females who use steroids and are concerned about water retention might choose to use Aromasin at a low dose of just half a tablet twice per week, adjusting as necessary and many women will find even this amount is at the high end. This equals 12.5mg per dose with a 25mg tablet.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromasin Dosage for Increased Endogenous Testosterone Secretion and PCT\u003c\/div\u003e\n\u003cdiv\u003eIt’s known that Aromasin can stimulate the release of luteinizing hormone and follicle stimulating hormone which are both required for testosterone production. But the very dramatic and effective way that Aromasin can suppress estrogen can in fact be its downfall for PCT use, where you do need some low level of estrogen as a male for testosterone to start normalizing again. Therefore, SERMs like Nolvadex and Clomid are mostly recommended for PCT instead.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome people will combine both that SERM and the AI Aromasin for PCT, and while studies have shown a SERM-AI combination can be counterproductive using other aromatase inhibitor products, this does not seem to be the case with Aromasin. A maximum dosage of 25mg daily for Aromasin during PCT for 2 weeks can be combined with Nolvadex at up to 40mg daily for 4 weeks as an effective PCT cycle – however many men will find that the SERM alone is enough to adequately recover testosterone function and retain your gains.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAROMASIN vs NOLVADEX FOR PCT\u003c\/div\u003e\n\u003cdiv\u003eThe two main goals of PCT are to help your testosterone recovery and to retain the gains you’ve made on your steroid cycle. Both Aromasin and Nolvadex are both known to work very well to reduce your estrogen levels and associated side effects while you’re using steroids – but what about after your steroid cycle during post cycle therapy?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe SERM Nolvadex is possibly the most used drug for post cycle theraphy to stimulate testosterone production and help get your normal hormonal function back on track following the extreme testosterone suppression that steroids cause. In addition to helping lower your circulating estrogen levels while you’re on a steroid cycle, Aromasin has the other beneficial effect of stimulating natural testosterone production and this can make it appealing for PCT purposes.\u003c\/div\u003e\n\u003cdiv\u003eOne of the standout factors of this AI compared to some of the older (though still popular) products like Arimidex is that it can also increase Insulin-Like Growth Factor-1 (IGF-1) which is something that other AIs are not known to be able to do. This increases your overall anabolic state which is going to be critical for maintaining your gains, which can easily fall away after your steroid cycle if you descend into a more catabolic state where muscle tissue is lost.\u003c\/div\u003e\n\u003cdiv\u003eSo while this looks to make Aromasin a very appealing PCT choice, it’s not quite that simple and in fact the very potent estrogen lowering effect of Aromasin can prove to be its downfall for PCT use – while we certainly don’t want higher than normal estrogen levels (men should always have a very small amount), suppressing it completely or to extremely low levels like Aromasin does can result in a great difficulty in testosterone production going back to normal levels because that process does require some amount of estrogen and it’s very possible to Aromasin is just too powerful in the estrogen suppression process to be of great use during PCT.\u003c\/div\u003e\n\u003cdiv\u003eTherefore, a SERM like Nolvadex is most often used and recommended for PCT over the AI Aromasin. For most anabolic steroid users besides the most hardcore and advanced, Nolvadex is all you will often need, and an AI may not be necessary at all even though more and more steroid users are claiming that AIs are essential especially for controlling water retention.\u003c\/div\u003e\n\u003cdiv\u003eThis side effect can and should be addressed by the diet as well and with some effort most steroid users can find that the use of Aromasin during PCT is not necessary at all or only required at very low doses. Aromatase inhibitors are best used where they provide the most benefit, and that’s during a steroid cycle to protect against both estrogenic and progestin side effects.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740590694692,"sku":null,"price":510.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_abbac86c-af14-43aa-bd7d-32189066b2b3.jpg?v=1778054061"},{"product_id":"keifei-tren-hex-100","title":"Keifei Tren Hex 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eChemical Name: Trenbolone Hexahydrobencylcarbonate\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: 100mg\/ml x 10ml multi doses vial and 100ml\/ml x 1ml single dose ampoule\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePresentation: 10ml multi dose clear vial with Keifei® wording imprinted on the side. 10ml x Trenbolone Hexahydrobencylcarbonate 100mg\/ml. Sealed with brown flip off cap imprinted with keifei® wording. Each vial comes with 1 sets of 10 digits authentication codes. 10 vials\/ box in a beige and brown colour outer box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e1ml single dose ampoule x Trenbolone Hexahydrobencylcarbonate 100mg\/ml. Each ampoule imprinted with 3 rings on top blue, brown, blue with a brown dot below. All wording is imprinted. Pack in 3 x ampoules or 10 ampoules of 5 ampoules per tray x 2 in plastics insert with Keifei® imprint on it.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe outer box contains 60 ampoules of 20 inner boxes of 3 Ampoules in beige and brown box. Each inner box pack of 3 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOr the outer box contains 100 ampoules of 10 inner boxes of 10amps in beige and brown box. Each inner box pack of 10 ampoules come with 1 set of 10 digits authentication codes paste on each inner box.\u003c\/div\u003e\n\u003cdiv\u003eParabolin - Hex 100 This is a well know trenbolone used to make by Negma in France (parabolan 75mg in 1.5ml). It contains long acting ester hexahydrobenylcarbonate, which extends the active of the drug for more than 2 weeks. This form is always been thought of as more suitable design for humus use, due to the less frequent injections. Trebolone hexahydrobenylcarbonate is a very potent androgen with strong anabolic activity. It is well suited for rapid buildup for strength and muscle mass. It provides acceptable results in a short period of time. The anabolic effect is often compare to d bol or testosterone. But Parabolin hex 100 will not convert to estrogen even at a high dosage. While using this drug, you will experience extremely potent mass or strength increase with no water retention. So the mass gain is hard and defined! It can also helps to bring about an incredibly hard, ripped physique and is an ideal product for competitive bodybuilder.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWe do not worry about estrogen related side effects while using this drug but watch of your kidney and liver. Other side effects during the cycle are oily skin, aggressive behavior, and acne and hair loss.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740671336740,"sku":null,"price":1300.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_916e836c-f5e7-4b60-ae65-bf8968f53edf.jpg?v=1778054210"},{"product_id":"keifei-masteron-prop-100","title":"Keifei Masteron Prop 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eDosage: 100mg\/ml x 10ml multi doses vial.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePresentation: 10ml multi dose clear vial. 10ml x Drostanolone Propionate 100mg\/ml. Sealed with flip off.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron 100 – This drugs which has a structure of moderate anabolic and low androgenic which does not aromatize to estrogen. Water retention and gynecomastia are not a concern while using this drug. Bodybuilders have a strong appreciation for non aromatizing androgens, find Mastbolin 100 very useful as a cutting agent. It uses a number of weeks prior to a competition as it will help to sharpen the their physic while dieting Recreational users might also interested with this item as it is an anabolic effect which will providing a consistent gain for high quality muscle. When it uses with Nandrolin 250 or Equipbolin 200, users may experience solid muscle gain without excessive water retention. While it stacks with Testosterone or D bol will experience an extreme muscle gain with lower water retention and other estrogenic side effect. Side effect is a mild for this drugs, no concern for gynecomastia or water retention. So are problems controlling blood pressure usually associated with estrogen. Mastbolin 100 is not liver toxic during this cycle so little stress will be placed on this organ. Basic androgenic side effects are oily skin, acne, body or facial hair growth, aggression and accelerated hair loss.\u003c\/div\u003e\n\u003cdiv\u003ehttps:\/\/en.wikipedia.org\/wiki\/Drostanolone_propionate\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrostanolone is an anabolic-androgenic steroid of the dihydrotestosterone group that was never marketed. It is considered a medium or mild strength steroid and is distributed under the brand name Masteron. The steroid comes in two variants: Propionate and Enanthate. Masteron Enanthate is the same anabolic steroid as Masteron Propionate; the hormone itself has not been changed. The only difference in the two compounds is the attached ester, which affects the drug’s active life and release into the body. Although this steroid is used by bodybuilders and athletes, it is not nearly as popular as Masteron Propionate. Masteron Enanthate, commonly known as Drostanolone Enanthate is a DHT based steroid. Drostanolone is just the DHT hormone structurally altered. The alteration exists through the addition of a methyl group at carbon position 2. This ensures the hormone doesn’t suffer metabolic breakdown brought on by the 3-hydroxysteroid dehydrogenase enzyme found in the skeletal muscle. This simple structural change also makes the hormone far more anabolic, and that gives us Drostanolone. Enanthate is not a steroid or a drug but nothing more than a timing tool used for a drug.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrostanolone or Masteron is an exotic androgenic steroid of the dihydrotestosterone group that was never marketed. Masteril was the brand name when it was first developed and was used then to help improve breast cancer. Being that this compound is derived from dihydrotestosterone, or DHT, it does not aromatize. Aromatization is the process of a compound being converted to estrogen in the body. Masteron is a very useful steroid because of this benefit. Many bodybuilders use it for preventing the aromatization of other steroids that are known to convert into estrogen. It is considered a medium or mild strength steroid and is distributed under the brand name Masteron now. The steroid comes in two variants: Propionate and Enanthate.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740773998884,"sku":null,"price":790.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_9d06738e-1a5d-49e7-8d09-2ec1574931c6.jpg?v=1778054346"},{"product_id":"keifei-test-mix-325","title":"Keifei Test Mix 325","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI TESTABOLIN 325(325MG\/ML 5 TESTOSTERONE MIX=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 3 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic steroid (For injection) Average Reported Dosage: Men 125-2000mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low except in high dosages over 1000-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Significantly after 2 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSustaject 325 is a mixture of the 5 testosterone esters:                     \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eACETATE -30mg\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePROPIONATE -50MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePHENYLPROPIONATE -50MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCYPIONATE -90MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDECANOATE -100MG \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is a well structured product that acts as a well timed time-released high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic\/high androgenic testosterone. In fact, due to TESTOSTERONE PROPIONATE,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ethis product becomes active after one day, but through the series of the other 3 testosterones, remains active for 3 weeks. This mixture had a reported better over all effect milligram for milligram than any other testosterone alone. Users experienced a rapid increase in strength and an even increase in solid mass during administration. SUSTANON aromatized less and caused less water retention when compared to other single testosterones and much less than OMNADREN. Liver toxicity was low (Except in ridiculous dosages) as the liver metabolizes testosterone very efficiently. Like all testosterones, SUSTANON provided improved muscle pumps, better post-training recuperation, and an elevation in aggressiveness toward training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSUSTANON 250\u0026amp;TEST COMBO 300 significantly suppressed the HPTA so natural testosterone production was significantly decreased as well. For this reason, HCG and CLOMID were considered mandatory after 4-6 weeks of continuous use and after the discontinuance of the drug.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales normally utilized dosages of 250-1000mg weekly, but some used higher dosages. As a rule, excellent results were realized with a dosage of 250-500mg every 7­10 days. Most novices and women noted that they felt that they should not use testosterone. Novices…because it was not necessary and it will limit later potential progress. Women should not use them (but a few reported doing so) due to virilizing effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome woman polled just could not leave testosterones alone. PROSCAR (FINASTERIDE, A DHT BLOCKER) was considered mandatory for co-administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eand TESTOSTERONE PROPIONATE 50mg 1 time weekly was noted to cause less virilizing side effects.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740863979812,"sku":null,"price":620.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c8337427-b659-40b7-8206-c1d9ead4ea8f.jpg?v=1778054452"},{"product_id":"keifei-cjc-1295-with-dac","title":"Keifei CJC-1295 with DAC","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cspan\u003ePresentation: Each 2ml multi dose vial contains 2 mg\/vial with Keifei® wording imprinted on the side. Orange colour cap with keifei® wording stamp on it. Come in both 10 x 2mg\/vial with 10 x 2ml\/ampoules of Bacteriostatic Water in a plastic insert in white and orange colour box. 1 set of 10 digits authentication codes paste on the plastic tray.\u003c\/span\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCJC-1295 is a Long-acting growth-hormone-releasing hormone (GHRH) analog. Because of the long half-life and stability of the CJC-1295 analog, it appears to become more and more popular. CJC-1295 is a Long acting GHRH analog. Growth-hormone-releasing hormone (GHRH), also known as growth-hormone-releasing factor (GRF or GHRF) or somatocrinin, is a 44-amino acid peptide hormone produced in the hypothalamus by the arcuate nucleus. GHRH stimulates growth hormone (GH) secretion from the pituitary. GHRH is released in a pulsatile manner, stimulating pulsatile release of GH respectively. In addition, GHRH also promotes slow-wave sleep.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe active portion of this GRF or GHRH peptide can be found as a 29 amino acid long peptide and is appropriately named GHRH1-29. This pulsatile release of various peptides is due to the negative feedback loop that is part of the hGH axis and controls the amount of hGH that your body produces to keep it in a homeostatic environment. Despite the effectiveness of GHRH to stimulate growth hormone release there are a number of problems associated with using it in vivo. The most noteworthy problem is the half life of the peptide, which has been shown to be ~7 minutes using advanced HPLC technologies that have proven to be very accurate. The reason for this relatively short half life is due to an enzyme called dipeptidylaminopeptidase IV (DPP-IV), which has a high affinity for the amino acids Ala and Pro and in the case of GHRH it cleaves the 1 and 2 positions that consist of Tyr-Ala, creating GHRH3-29, an inactive form of the peptide. To prevent the problems associated with natural GHRH, pharmaceutical companies looked at new ways to increase the half life and bioavailability of these smaller peptides with technologies that work far different than other technologies, such as Pegylation.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCJC-1295 is a synthetic modification of growth hormone releasing factor (GRF) with D-Ala, Gln, Ala, and Leu substitutions at positions 2, 8, 15, and 27 respectively. These substitutions create a much more stable peptide with the substitution at position 2 to prevent DPP-IV cleavage, position 8 to reduce asparagine rearrangement or amide hydrolysis to aspartic acid, position 15 to enhance bioactivity, and position 27 to prevent methionine oxidation. By applying the Drug Affinity Complex (DAC) technology to GRF, the peptide selectively and covalently binds to circulating albumin after subcutaneous (SC) administration, thus prolonging its half-life. These substitutions are key in increasing the overall half life of CJC-1295 but there lies an even greater reason as to why the half life has been extended from ~7 minutes to greater than 7 days!\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBioconjugation is a relatively newer technology that takes a reactive group and attaches it to a peptide, which in turn reacts with a nucleophilic (usually a partially negative molecule) entity found in the blood to form a more stable bond. Albumin, one of the most abundant substances in the human body is chosen as the nucelophile by this particular peptide thanks to a Cys34 thiol group that attracts it. By combining the tetrasubstituted GHRH analogue with maleimodoproprionic acid using a Lys linker, you create a GHRH peptide with a high binding affinity for albumin. Once the CJC-1295 molecule has attached itself to albumin, it is given an extended half life and bioavailability thanks to the albumin preventing enzymatic degredation and kidney excretion. In fact, bioconjugation is so effective that there was less than 1% of CJC-1295 left unreacted in vivo and over 90% was stabilized after subcutaneous injection. This means that you get more of what you paid for working for you. There was no DPP-IV degredation observed on CJC -1295 in any of the various experiments conducted.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53740931350820,"sku":null,"price":3150.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_e01de53e-06ac-4d48-9a44-449836dc64bc.jpg?v=1778054544"},{"product_id":"keifei-femara","title":"Keifei Femara","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cspan\u003eLike most of the AIs we look at for using alongside anabolic steroids, Letrozole (Femara) was also developed for the medical treatment of breast cancer in post-menopausal women.\u003c\/span\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe reason it is only used in women of such an age is due to its powerful estrogen blocking ability which would have serious health implications for pre-menopausal women, but for male steroid users it is this trait that makes AIs like Letrozole (Femara) so appealing as we aim to combat the adverse effects of estrogen when using aromatizing steroids.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLetrozole can lower your overall estrogen levels because it blocks the aromatase enzyme. This contrasts with the other popular category of estrogen control drugs for steroids users, SERMs, which only target very specific areas of the body. This allows Letrozole to combat a wider range of estrogenic side effects caused by steroids, with the two main ones being gynecomastia and water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis will also help prevent the high blood pressure that can come along when excess water retention is not addressed.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage Instructions\u003c\/div\u003e\n\u003cdiv\u003e1.25mg-2.5mg \/day\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEven at very low doses Letrozole is a potent drug so you do not require a lot of it to benefit from its full effects. Unlike with many of the other AIs or SERMs you might use as a steroid user where doses are normally higher than those used for medical treatment, with Letrozole we can get away with using a similar dose or even lower than is administered when the drug is used medically.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLetrozole Dosage During Anabolic Steroid Use\u003c\/div\u003e\n\u003cdiv\u003eMaking the mistake of taking too much Letrozole during steroid use will have no benefit and bring about negative effects, like fatigue. So, it’s critical to maintain a sensible dose.\u003c\/div\u003e\n\u003cdiv\u003eWith a medical dose usually around 2.5mg daily, we would look at no higher than that and most of the time even lower. To protect from estrogen related side effects during steroid use a dose of as low as 0.5mg to 1.25mg every two days is often enough for excellent estrogenic related protection for most men.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOnly if you are experiencing early signs of gynecomastia would increasing the dose at this time up to 2.5mg per day can potentially even fully reverse the symptoms; but be prepared for a noticeable zap in energy during this time. Once gyno symptoms subside it’s important to reduce your Letrozole dose back down to regular estrogenic protection levels.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFemale Letrozole Dosage\u003c\/div\u003e\n\u003cdiv\u003eIncreased estrogen levels are not anywhere near as great a concern for female steroid users as it is for males. The main reason for using an AI like Letrozole by females would be to mitigate water retention, especially for competitive bodybuilders or physique athletes where this is most important.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn fact, Letrozole is not recommended as a first choice for females due to its potency in reducing estrogen so much, hence why it is not used medically by females who have not gone through menopause. Females who are determined to use this AI are advised to dose at just 0.5mg every other day and gauge results and effects from there.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLetrozole Dosage for Increased Endogenous Testosterone Secretion and PCT\u003c\/div\u003e\n\u003cdiv\u003eThis AI may have some ability to raise testosterone levels mainly through its ability to reduce estrogen. Both luteinizing hormone and follicle stimulating hormone have shown to be able to be increased by Letrozole and these are essential to the production of testosterone.\u003c\/div\u003e\n\u003cdiv\u003eSo, while a reduction of estrogen is important for bringing about a rise in testosterone levels, this is a fine balance in men and reducing estrogen too low can actually have the opposite effect with testosterone not able to increase to a normal level if estrogen is suppressed too powerfully, which Letrozole has the ability to do.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFor this reason, many will choose not to make use of this drug during post cycle therapy at all, in favor of using a SERM like Nolvadex. However, if you find that Letrozole is preferable for you for post cycle therapy use, a low dose similar or lower to that stated above for during your steroid cycle is the only way to reduce the risk of very low estrogen occurring.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMaking use of Letrozole alongside Nolvadex, which is a staple in PCT for most men, results in both drugs making the other less effective. Combining these drugs is not recommended for PCT and therefore most people will opt simply to use the better PCT option in the SERM Nolvadex while enjoying the benefits that Letrozole can provide during the steroid cycle only.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741011501348,"sku":null,"price":460.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_57b1c0a3-3ec7-4702-8f65-e527645fc2d1.jpg?v=1778054671"},{"product_id":"keifei-t3-100-tabs-25mg","title":"Keifei T3 100 Tabs 25mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eLiothyronine is a form of thyroid hormone used to treat hypothyroidism and myxedema coma. Liothyronine is the most potent form of thyroid hormone. Chemically, it is nearly identical to triiodothyronine(T3). As such, it acts on the body to increase the basal metabolic rate, effect protein synthesis and increase the body's sensitivity to catecholamines (such as adrenaline) by permissiveness. The thyroid hormones are essential to proper development and differentiation of all cells of the human body. These hormones also regulate protein, fat, and carbohydrate metabolism, affecting how human cells use energetic compounds.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn comparison to levothyroxine (T4), liothyronine has a faster onset of action as well as a shorter biological half-life, which may be due to less plasma protein binding to thyroxine-binding globulin and transthyretin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrugs with thyroid hormone activity, alone or together with other therapeutic agents, have been used for the treatment of obesity. In euthyroid patients, doses within the range of daily hormonal requirements are ineffective for weight reduction. Larger doses may produce serious or even life-threatening manifestations of toxicity, particularly when given in association with sympathomimetic aminessuch as those used for their anorectic effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhysicians can use this instead of or in addition to levothyroxine (T4) for patients undergoing thyroid withdrawal. When a patient has thyroid cancer or Graves' disease, ablation therapy with radioactive iodine (131I) can be used to remove any trace thyroid tissue. For 131I therapy to be effective, the trace thyroid tissue must be avid to iodine. The best method is to starve the tissue of iodine but this can lead to hypothyroid symptoms for the patient. Withdrawal from levothyroxine can be done but it takes six weeks of withdrawal for the remaining thyroid tissue to be completely starved. Six weeks is needed owing to levothyroxine's long half life. Six weeks can be inconvenient for the patient and delay treatment. Liothyronine instead can be taken and withdrawn from for two weeks to starve the thyroid tissue. This is much safer and more convenient than levothyroxine.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiothyronine may cause a number of side effects, mostly similar to symptoms of hyperthyroidism, which include:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e- weight loss\u003c\/div\u003e\n\u003cdiv\u003e- tremor\u003c\/div\u003e\n\u003cdiv\u003e- headache\u003c\/div\u003e\n\u003cdiv\u003e- upset stomach\u003c\/div\u003e\n\u003cdiv\u003e- vomiting\u003c\/div\u003e\n\u003cdiv\u003e- diarrhea\u003c\/div\u003e\n\u003cdiv\u003e- stomach cramps\u003c\/div\u003e\n\u003cdiv\u003e- nervousness\u003c\/div\u003e\n\u003cdiv\u003e- irritability\u003c\/div\u003e\n\u003cdiv\u003e- insomnia\u003c\/div\u003e\n\u003cdiv\u003e- excessive sweating\u003c\/div\u003e\n\u003cdiv\u003e- increased appetite\u003c\/div\u003e\n\u003cdiv\u003e- fever\u003c\/div\u003e\n\u003cdiv\u003e- changes in menstrual cycle\u003c\/div\u003e\n\u003cdiv\u003e- sensitivity to heat\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741100728612,"sku":null,"price":370.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_4bb32b01-e4b5-4aee-a9da-044894be0f0a.jpg?v=1778054814"},{"product_id":"keifei-ment-100","title":"Keifei Ment 100","description":"\u003cp\u003e\u003cspan\u003eChemical Name: Trestolone Acetate\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: 100mg\/ml x 10ml multi doses vial\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePresentation: 10ml multi dose vial with keifei® wording imprinted on the side. 10ml x Trestolone Acetate 100mg\/ml. Sealed with light greenish blue flip off cap with keifei® wording imprinted. Each vial come with 1 sets of 10 digits Authentication Code. 10 vials\/ box in a white and light light greenish blue box.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSuperbolin is a potent anabolic steroid. Also referred to as 7 alpha-methyl-19-nortestosterone (MENT), it is a synthetic steroid that is considered extremely powerful in the body, surpassing the strength of testosterone. It is considered beneficial for the purpose of bodybuilding and strength training, but it comes with a price.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrestolone Acetate, while used for other medically-related purposes, is a popular alternative for the individual who is serious about perfecting the human physique. It is recognized for its fast and effective results for anyone who is looking for rapid strength enhancement and is serious about increased size in as little time as possible. Trestolone Acetate is intended for dedicated bodybuilders and weight trainers who are committed to getting positive results through a combination of diet, supplements, and a fitness regimen\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrestolone Acetate has an edge over the competition due to the fact that it is extremely powerful. In addition, it is based on sound, MEDICAL RESEARCH, NOT FOR HUMAN COMPSUMPTION. While other steroids require testosterone supplementation as well, Trestolone Acetate can be used independently. It is considered an optimal drug for achieving muscle growth as compared to its counterparts.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741146865956,"sku":null,"price":1330.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_af35d97e-181a-4d04-8b8d-20f452e7b6c2.jpg?v=1778054929"},{"product_id":"keifei-tren-blend-200","title":"Keifei Tren Blend 200","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI PARABOLIN BLEND 200(200MG\/ML TRENBOLONE BLEND=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD NANDROLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 2-3 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (for injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 30-60 mg every other day\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Though disputed, yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eKidney Toxic: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: High Anabolic\/Very high Androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eandrogenic 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003estandard nandrolone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 8-10 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (for injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-400 mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Though disputed, yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eKidney Toxic: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: High Anabolic\/Very high Androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eandrogenic 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003estandard nandrolone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 5-7 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic Steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Dosage: Men: 76-228-mg weekly; Women: 76-mg weekly (but should not use)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Rare, usually none\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ehighly toxic to kidneys also\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBLEND OF 3 TREBELONES.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis was\/is a very nasty but effective steroid that was removed from the market about 1987 or so. Not all that long ago it began showing up on the black market from Australia. Upon testing the 50-ml vials, it was discovered that it actually contained 31-mg\/ml of Trenbolone acetate. Most Fina Jet now found is bogus. It contains either a testosterone ester, ground Finaplix pellets, or just oil. But the original has been discontinued. (There are several new brands of the drug trenbolone acetate)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone acetate is a strong androgenic\/anabolic steroid that caused a fast increase in strength and increased fat burning if the athlete’s diet was right. Unless stacked with other steroids, this drug did not cause much in actual weight gain (dose dependent). Its main use was to harden the physique’s appearance once body fat levels were low enough before competition. For the most part, bodybuilders have replaced Finajet\/ Finaject with Parabolan or one of the many black market trenbolone products. Since Finajet did not cause gyno or water retention, one may assume it was fairly clean. Wrong! Even at dosages of 30-60-mg injected daily, side effects such as kidney toxicity, nose bleeds, headaches, high blood pressure, acne, and serious attitude problems were common.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome creative and brave athletes have used the Finaplix 20 mg pellets which are intended for animal use. The pellets are shot into animal tissue for a slow release of Trenbolone. However some athletes (and black market crazies) have ground the pellets into a powder, mixed it with oil or water, and injected the very un-sterile solution with 18 gauge needles. I can not stress enough how dangerous this is. The product is often labeled Finabolan. (“Finabolin” gives us a chance to discuss trenbolone in greater depth in a moment)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnother reported method of using the Finaplix pellets was to ground them into powder, mix the powder with a 50\/50 solution of DMSO (DIMETHYL SULFOXIDE) and water. Then apply it to skin. The DMSO acts as a transporter that allows 14-18-MG of a 20MG pellet to be absorbed into the blood stream while the skin acts as a filter of sorts. Unfortunately this also allowed many toxins on the skin to enter as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome individuals have claimed real hard-core status by using an animal pellet implant gun and taking one in the glute. Do not try this at home. The pain would be major and compared to being shot with a .177 pellet. The interesting side of this is that the lads who did this had been told that the Finaplex pellets were readily absorbed “rectally”.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Geez! And some bodybuilders wonder why we have the stigma of dull wittedness?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNOTED POSITIVE EFFECTS OF TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Amazing anabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Rapid high quality lean tissue gains. (Dose dependent) *Maximum post-cycle lean mass retention. *Low-none water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased Erythropoies (Red blood cell production) *Does not aromatize to estrogens. *Superior strength and mass gain. (Lean) *Extreme hardening of musculature and vascularity. *Excellent protein sparing\/anti-catabolic qualities. *Reduction in fat stores and favorable distribution. *Increased metabolic rate. *Low-moderate HPTA function inhibition. *Significant increase in muscle glycogen synthesis. *Increase creatine phosphate (CP) synthesis. *Improved muscle insulin receptor activity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Remains anabolic during calorie restricted periods. (High protein intake remains necessary)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e POSSIBLE NEGATIVE EFFECTS TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Liver and Kidney toxicity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Growth of prostate tissue. (PSA test is wise)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Male pattern baldness. (Accelerated genetic predisposition)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Mild hallucinations. (High dosage -prolonged use)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*High blood pressure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e Trenbolone Acetate is a fast acting injectable steroid.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTo increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate ,enanthate or Hexahydrobenzylcarbonate. Trenbolone is then produced as a metabolite by the reaction of these compounds with the androgen receptor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg\/week up to 1400 mg\/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5α-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom\/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741278822692,"sku":null,"price":1330.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c7ba3d49-a391-4249-96f8-409c993f2763.jpg?v=1778055089"},{"product_id":"keifei-bpc-157","title":"Keifei BPC-157","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI BPC 157(PENTADECAPEPTIDE 5MG=1 POWDER+WATER))\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBPC 157 (Body Protection Compound-157) is a pentadecapeptide made up of 15 amino acids. The amino acids sequence in BPC 157 is similar to a portion of the human BPC amino acid sequence. Human BPC is found in the gastric juice. Experiments have shown that BPC 157 enhances the healing of wounds, including tendons wounds such as transected Achilles tendons of rats. The aim of this study was to investigate the probable mechanism that BPC 157 utilizes to accelerate the healing process in an injured tendon. The study used two group of tendon explants of which one group was cultured in a BPC 157-containing medium while the other group was cultured in a medium lacking BPC 157. These cultures were thereafter examined for tendon fibroblasts outgrowths. Such outgrowths indicated tendon regeneration.The results revealed that the explants’ outgrowth was significantly accelerated in the culture containing BPC 157 as compared to the culture lacking BPC 157. Also, a MTT assay did show that BPC 157 does not directly affect cellular proliferation in a culture of rat-derived Achilles tendon. However, results also showed that BPC 157 significantly increased the survival of cells under oxidative stress. Furthermore, the Transwell filter migration assay showed that BPC 157 significantly increased in-vitro fibroblast migration in a dose-dependent fashion. Moreover, BPC 157 accelerated the dispersal of the fibroblasts in culture dishes in a dose-dependent manner\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdditionally, FITC-phalloidin staining was able to demonstrate that BPC 157 induces F-actin formation in fibroblasts. Likewise, Western blot analysis was able to detect the production and activation of paxillin and FAK proteins. The western blot analysis also showed that BPC 157 increases the extent of phosphorylation of paxillin and FAK proteins without affecting the amounts produced.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThus, it can be concluded that BPC 157 enhances the ex-vivo growth and in-vitro cellular migration of fibroblasts derived from rat tendon explants. Moreover, BPC 157 also increases the probability of a cell surviving under oxidative stress. These actions of BPC 157 are probably mediated by the activation (through phosphorylation) of the proteinic FAK-paxillin pathwa\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741372866852,"sku":null,"price":1330.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_f3d1fcfd-9794-47e9-aafd-8e6185d30be8.jpg?v=1778055238"},{"product_id":"keifei-tb500","title":"Keifei TB500","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI TB500(5MG=1 POWDER+WATER)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThymosin Beta 4, or TB-500, is a synthetic version of a naturally occurring 43-amino acid peptide present in nearly all human and animal cells studied.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA 2010 study in the Annals of the New York Academy of Sciences supported TB500’s potential for cardiac muscle repair following injury, eg, after myocardial infarction (heart attack). Recognizing the limitations of stem cell therapy for this application, TB500 was found to inhibit myocardial cell death, stimulate blood vessel growth, and activate cardiac processes that encouraged the heart to heal following injury. The investigation showed that TB500 may be the first agent which can actively recover injured cardiac muscle following heart attack. This is further supported with prior mouse studies in 2004 showing cardiomyocyte migration, survival and repair of myocardial damage. [1] [2]\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFilamentous actin (F-actin, or actin) forms polymers that thicken sputum, adversely affecting cystic fibrosis patients. TB500 was studied in a population of CF patients, showing a dose- and time-dependent decrease in cohesivity of sputum after administration of TB500 when combined with dornase alfa. The combination therapy showed a 71% improvement in mucociliary transport of mucus, and a 44% improvement in cough transport of mucus. [3\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTB500 is known to stimulate myoblasts and myocytes (muscle generating cells). Mitochondrial RNA levels of TB500 have been shown to increase following muscle injury, helping to regenerate muscle fibers and address inflammation in the injured location. The data support muscle injury causing increased local production of TB500, promoting migration of incoming myoblasts to accelerate skeletal muscle regeneration. [4]\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTB-500 is a synthetic version of the naturally occurring peptide present in virtually all human and animal cells, Thymosin Beta 4 (Tß4). It is a first-in-class peptide candidate that promotes the following*: Endothelial (blood vessels) cell differentiation Angiogenesis (growth of new blood cells from pre-existing vessels) in dermal tissues Keratinocyte migration Collagen deposition; and Decreases inflammation.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTB-500 offers many benefits to the equine world in performance racing. Recent trials by some of the world’s leading trainers on their prize winning equine members of both genders, have been credited by a huge boost in their race-day results, something long desired in the racing world. These trials along with clinical trials have indicated the following benefits associated with the use of TB-500 on mares and stallions: Increase muscle growth with huge increases in endurance and strength noted Relaxed muscle spasm Improved muscle tone Increase the exchange of substance between cells Encourage tissue repair Stretches connective tissue Helps maintain flexibility Reduces inflammation of tissue in joint Enhances nutritional components in the animal Prevents the formations of adhesions and fibrous bands in muscles, tendons and ligaments. When these proven benefits are viewed in conjunction with the fact that 60% of a horse’s body weight is muscle, it is clear to see the full potential of TB500 can be reviled in by majority of the horse’s body. In a racing era that surrounds itself around gaining that competitive edge through the use of various substances, none will deliver the results that will be experienced with the use of TB-500. Perhaps the greatest selling point of the product is that it’s 100% DRUG FREE and DOES NOT SWAB. This allows the peptide to be used right throughout racing spells in both training and competition completely free of any banned substance.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTB-500 dosage and cycle duration:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage depends on the purpose and severity of the injury \/ damage you are treating. People generally use between 4 to 8 mg of TB500 per week during the initial (loading) period of 4 to 6 weeks. Afterwards some opt to maintain the effects with a low 2 to 6 mg dose once every 2 weeks. The effects of TB-500 wear off within 2 – 3 weeks of injection.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e1. TB-500 loading phase:\u003c\/div\u003e\n\u003cdiv\u003eduration: between 4 – 6 weeks\u003c\/div\u003e\n\u003cdiv\u003edosage: between 4 – 8 mg of TB-500 per week\u003c\/div\u003e\n\u003cdiv\u003efrequency of injection:2 mg per injection, between 2 – 4 times per week (depending on the total weekly dosage)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e2. TB-500 maintainance phase:\u003c\/div\u003e\n\u003cdiv\u003eduration: as long as needed\u003c\/div\u003e\n\u003cdiv\u003edosage: between 2 – 6 mg of TB-500 per 2 weeks\u003c\/div\u003e\n\u003cdiv\u003efrequency of injection:2 mg per injection, between 2 – 3 times per 2 weeks (depending on the total bi-weekly dosage)\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741473005860,"sku":null,"price":2000.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_8b8508ef-fac2-4175-a40c-8f44b5371221.jpg?v=1778055373"},{"product_id":"keifei-melanotan-2-inject","title":"Keifei Melanotan 2 - Inject","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cspan\u003eKeifei MELANOTAN 2(10MG\/2ML VIAL)\u003c\/span\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMelanotan 2 (also referred to as Melanotan II) is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis, a process responsible for pigmentation of the skin. This peptide hormone, called alpha-Melanocyte stimulating hormone or MSH, activates certain melanocortin receptors in the process of exerting its effects. Indeed, MSH also exerts potent influence over lipid metabolism, appetite, and sexual libido via these melanocortin receptors. As a result, Melanotan 2 has been shown in studies to exhibit appetite suppressant, lipolytic, and libido-enhancing effects in addition to promoting skin tanning. Melanotan 2 has been researched extensively for use in protecting against the harmful effects of ultraviolet radiation from sunlight due to its melanogenesis-stimulating properties.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdditionally, Melanotan 2 and a similar synthetically produced variant, known as PT-141, have been studied at length as a potential remedy for the treatment of sexual dysfunction; specifically, male erectile dysfunction.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMelanotan II Dosage Frequency\u003c\/div\u003e\n\u003cdiv\u003eThe frequency of Melanotan II injections depends on the phase of usage you are in. If you are new to the product or are taking it again for the first time after a period of absence, then you will begin with what is called the “loading phase” and will need to inject every day. Once you have achieved the shade of tan you are happy with, then you can switch to the “maintenance phase” which involves less frequent injections.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLoading Phase\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow often: One injection, taken every day (7 times per week) For How Long: Until you have achieved your desired shade of tan (this will take 2-6 weeks depending on how often you tan and your skin type).\u003c\/div\u003e\n\u003cdiv\u003eMaintenance Phase\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow often: One injection taken 2 or 3 times per week.\u003c\/div\u003e\n\u003cdiv\u003eFor How Long: If you want to maintain your shade of tan. Upon cessation of usage, your skin will return to its natural shade in about 1-2 months.\u003c\/div\u003e\n\u003cdiv\u003eTanning Frequency\u003c\/div\u003e\n\u003cdiv\u003eDespite being referred to us a “sunless tanning” agent, Melanotan II (MT2) requires UV exposure to work properly, results without it develop extremely slowly or sometimes not at all. The incidence of side effects such as hyperpigmentation also appears to be higher when Melanotan II is taken on its own and without exposure to the sun or sun beds.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUV exposure recommendations\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLoading Phase: 2-3 times per week if you wish to develop your tan as quickly as possible, otherwise once per week will allow your tan to build gradually.\u003c\/div\u003e\n\u003cdiv\u003eMaintenance Phase: 1 tanning session per week is usually sufficient to maintain your color. For How Long: 5-10 minutes in a sunbed (solarium) or 20-40 minutes in the sun.\u003c\/div\u003e\n\u003cdiv\u003ePrecautions: Do not overexpose yourself to the sun, whilst Melanotan II does reduce sunburn, it only does so by approximately 50% for most users. Therefore, it is still wise to apply sunscreen, especially on sensitive areas. Sunscreen will not affect Melanotan II’s ability to give you a tan.\u003c\/div\u003e\n\u003cdiv\u003eTanning Results\u003c\/div\u003e\n\u003cdiv\u003eIf your tan is not developing as quickly as you’d like, then you simply need to increase the frequency of your UV exposure. You should never increase your Melanotan II dosage or injection frequency.Melanotan II and UV exposure complement each other, so if you spend a lot of time tanning you will need less frequent injections of Melanotan II to obtain and maintain your tan. If you don’t spend much time in the sun or sun beds, then you will need more frequent dosages of Melanotan II to develop and keep your tan\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects include:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDarkened skin\u003c\/div\u003e\n\u003cdiv\u003eIncreased moles and freckles\u003c\/div\u003e\n\u003cdiv\u003eNausea\u003c\/div\u003e\n\u003cdiv\u003eVomiting\u003c\/div\u003e\n\u003cdiv\u003eLoss of appetite\u003c\/div\u003e\n\u003cdiv\u003eFlushing of the face\u003c\/div\u003e\n\u003cdiv\u003eInvoluntary stretching and yawning\u003c\/div\u003e\n\u003cdiv\u003eSpontaneous erections\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741563674916,"sku":null,"price":390.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_b4411db6-478f-4d84-bc35-1499bdd69061.jpg?v=1778055478"},{"product_id":"keifei-hcg-pregnyl","title":"Keifei HCG - Pregnyl","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI PROGONA 5000(5000IU CHORIONIC GONADOTROPIN\/AMP=3 POWDER+WATER)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePregnyl (chorionic gonadotropin) is a hormone used to cause ovulation and to treat infertility in women, and to increase sperm count in men. Human chorionic gonadotropin (HCG) is also used in young boys when their testicles have not dropped down into the scrotum normally. – Human Chorionic Gonadotropin – is the active ingredient used in “Pregnyl”.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is typically used as part of a PCT to “reactivate” ones natural production of testosterone post cycle. When on a heavy, long cycle it is also advisable to use it weekly at a low dose of 250 – 500iu to just keep the testicles active during the cycle. This helps with the “kick start” of natural production at the end of the cycle as the testicle will not be starting from a point of a prolonged period of zero \/ low activity.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741638189348,"sku":null,"price":850.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_4d0603ce-d627-4e1d-ba06-0aaa35fd54c0.jpg?v=1778055618"},{"product_id":"keifei-ghrp-6-10-vial-kit","title":"Keifei GHRP-6 10 Vial Kit","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI GHRP-6(5MG=10 POWDER+WATER))\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGHRP-6 is a potent stimulator of natural Growth Hormone release. GHRP-6 is a Hexa-peptide that promotes food intake by stimulating hunger and helps increase energy metabolism. Growth Hormone Releasing Peptides, similar to GHRP-6, are most commonly used for treatment of Growth Hormone (GH) deficiencies, eating disorders, obesity, etc. Research has shown that use of these HGH Peptides increases lean muscle mass, strength, stamina and decreases body fat.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe Development of GHRP-6\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn 1982, the natural hormone “Growth Hormone Releasing Hormone” (GHRH) was identified after a prolonged search. Soon, researchers discovered that those GH-Releasing Peptides (specifically GHRP-6 \u0026amp; GHRP-2) followed a mode of action which bound them to and was mediated through receptors different from those for GHRH. Furthermore, researches discovered that these GH-Releasing Peptides acted synergistically with the natural hormone Growth Hormone Releasing Hormone (GHRH), which is related to Sermorelin, in both laboratory animals and humans to produce large releases of Growth Hormone. In the 1980s, the first highly potent GH-Releasing peptide, GHRP-6, was developed. Due to a strong GH release response from the the peptide, it became the first member of a class called Growth Hormone secretagogues. GHRP-6 is a hexapeptide composed of 6 amino acids: L-Histidine, D-Tryptophan, L-Alanine, L-Tryptophan, D-Phenylalanine and L-Lysine. The “L” form of an amino acid is the naturally occurring form and often in the nomenclature the “L” is dropped. The “D” form does not occur in nature and is the isomeric form (i.e. mirror image) of the naturally occurring “L” form. GHRP-6 (His-D-Trp-Ala-Trp-D-Phe-Lys-NH2) is composed of both natural and isomeric forms of those 6 amino acids.This sequence provides a signal to the body to begin secreting Growth Hormone release while also blocking Somatostatin, a hormone that inhibits the release of Growth Hormone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGHRP6\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGHRP6 is a growth hormone releasing hormone. GHRP 6 is a true HGH secretagogue. Which means it stimulates the body’s own secretion of HGH. GHRP-2, GHRP-6 and Hexarelin are replaceable drugs and have similar mechanism of action. They do however have small differences and therefore different athletes have their preferences.GHRP-6 up to 100mcg has no increase of cortisol and prolactin levels.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePRODUCT DETAILS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e5000mcg per vial\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eConstitute\u003c\/div\u003e\n\u003cdiv\u003e1ml or 2ml of water (but with the small measurements we suggest you use 2ml) depending on the brand you use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage\u003c\/div\u003e\n\u003cdiv\u003e100mcg to 300mcg as many as 5 times a day. Usually between 3 to 5 times per day before meals. Always take your last injection at bedtime.If you mix your GHRP6 5000mcg with 2ml of water then a 100mcg dose will measure 4 ticks on your insulin syringe. Not 40 but the small 4 ticks.Because of the frequency of injections it would be best to use the insulin syringes with a 8mm x 30 gauge (0,30mm) needle on. This is the smallest needle you can get.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFunctions\u003c\/div\u003e\n\u003cdiv\u003eIncreases muscle mass and reduce body fat. Increases appetite but not as dramatically as GHRP-2. GHRP-6 keeps your endogenous (natural) GH production flowing. It also strengthens the joints, connective tissue and bone mass.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTIPS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGHRP2 and GHRP6 works best if coupled with CJC1295 to get the most out of the peptides.\u003c\/div\u003e\n\u003cdiv\u003eIntramuscular and subcutaneous routes lead to different onset times but roughly similar peaks and declines.\u003c\/div\u003e\n\u003cdiv\u003eIt can be used alone or in conjunction with Growth Hormone.\u003c\/div\u003e\n\u003cdiv\u003ePost-injection: 30 minutes post-injection is usually when GHRH stimulation of GH release is complete, meaning it’s safe to consume food\/beverages after this time without worrying that they will cause your injection to be less effective. Consuming a high protein\/carbohydrate meal at this time will create an insulin spike and therefore assist with the anabolic (muscle building) effects of GH. Those looking to burn fat should wait as long as possible before eating and when you do, only eat high protein, low fat and low carbohydrate meals to allow GH’s fat burning effects to last as long as possible.\u003c\/div\u003e\n\u003cdiv\u003eAlternatively you can inject it 1 to 1.5 hours after a meal.\u003c\/div\u003e\n\u003cdiv\u003eDo not combine GHRP-6 and GHRP-2 in a cycle. It has very similar effects with small differences and preferences from person to person.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741709984036,"sku":null,"price":2300.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_36e79904-5b19-4e96-94bd-293d033e95cd.jpg?v=1778055710"},{"product_id":"keifei-hgh-fragment","title":"Keifei HGH Fragment","description":"\u003cp\u003e\u003cspan\u003eThis human HGH Frag 176-191 is a tailored form of amino acids 176-191 at the C-terminal region of the human growth hormone aka HGH. It has been documented that the fat reducing properties of GH appear to be elicited by a small analog region of the C-terminus end of the GH molecule. This specific region consists of amino acids 176-191, from which it gets its name.ThisHGH Frag 176-191 works by mimicking the way endogenous GH regulates fat metabolism but without the negative side effects. Exogenous GH can specifically cause trouble for one’s blood sugar or endogenous growth hormone production. Just as unrefined GH, the HGH FRAGMENT 176-191 triggers lipolysis which in return inhibits lipogenesi. HGH Frag 176-191 has not been documented to effect on endogenous growth hormone or insulin resistance, unlike the actual full GH molecule. Mg per mg this FRAGMENT is stronger than the unrefined standard GH. The AA chain is about 7-10%of the full GH molecule and if this is actually the vital active site so that would explain why it’s so effective at delivering the benefits of standard GH. The nice thing about FRAGMENT 176-191 is the fact that it primarily eats away at adipose tissue, which is the nasty unwanted fat. The usual dosage for FRAGMENT GH is around 500mcg daily.\u003c\/span\u003e\u003cspan\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMore proof for for this HGH Frag 176-191 “Investigators at Monash University discovered that the fat-reducing effects of GH appear to be controlled by a small region near one end of the GH molecule. This region, which consists of amino acids 176-191, is less than 10% of the total size of the GH molecule and appears to have no effect on growth or insulin resistance. It works by mimicking the way natural HGH regulates fat metabolism but without the adverse effects on blood sugar or growth that is seen with unmodified HGH. Like unmodified GH, the HGH FRAGMENT 176-191 stimulates lipolysis and inhibits lipogenesis both in laboratory testing and in animals and humans. The HGH FRAGMENT does not appear to affect appetite.” Another study documented that in laboratory tests on fat cells from rodents, pigs, dogs, and humans, the HGH Frag 176-191 released fat exclusively from obese fat cells but not from lean ones, reduced new fat build up in all fat cells, enhanced the burning of fat. In rodents (rats and mice), HGH Frag 176-191 reduced body fat in obese animals but, increased fat burning without changing their diet or bringing about excess growth (as it does not increase IGF levels) or any other unwanted GH effect.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat is GH?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGrowth hormone also known as GH or HGH is a protein-based peptide hormone. It stimulates growth of bones and organs, cell reproduction and regeneration, stimulates fat loss. Growth hormone is a 191-amino acid, single-chain polypeptide that is produced, stored, and secreted by the somatotroph cells within the lateral wings of the front part of the pituitary gland. The main isoform of the human growth hormone is a protein of 191 amino acids and contains a molecular weight of 22,124 daltons. The structure of GH includes four helices necessary for proper interaction with the GH receptor. Interstingly, it has been discovered that GH is an antagonist to prolactin and chorionic somatomammotropin. Despite marked structural similarities between growth hormone from different species, only primate growth hormones have significant effects in humans because of the related DNA that we humans share with primates. HGH is produced and secreted from the front part of the pituitary gland in a pulsatile way throughout the day; surges of secretion of GH occur at 3 to 5 hour intervals. The plasma concentration of GH during these spikes can range from 5 to even 45 nanograms per decaliter. The largest and most expected of theseGH spikes occurs about an hour after the beginning of sleep. Otherwise there is wide variation between days and individuals. Nearly fifty percent of HGH secretion occurs during the third and fourth NREM sleep stages. Between the spikes base GH levels are low, usually less than 5 ng\/mL for most of the day and night. Additional analysis of the pulsatile profile of GH described in all cases less than 1 ng\/ml for basal levels while maximum spikes were situated around 10-20 ng\/mL. A number of factors are known to affect HGH secretion, such as age of course, gender, diet, exercise\/eustress, distress, and other hormones. Young adolescents secrete HGH at the around a whopping amount of 700 μg\/day, while healthy adults secrete HGH a measly 400 μg\/day. Since polypeptide hormones are not fat-soluble such as GH, they cannot penetrate the cell membrane of a muscle cell. GH exerts some of its effects by binding to receptors on its intended target cells, where it activates the MAPK\/ERK pathway. Through this mechanism GHdirectly stimulates splitting and multiplication of chondrocytes of cartilage. This is a great reason to use FRAGMENT GH while ontestosterone or TRT. GH also stimulates the production of IGF-1 through the JAK-STAT signaling pathway. The Liver is a major target organ of GH for this specific process and is the main site of IGF-1 production. IGF-1 has growth-stimulating effects on a wide variety of tissues as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eReasons for GH deficiency\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMany people suffer from Growth Hormone Deficiency which is howGH therapy came about before they started promoting GH for its anti aging properties. There are many causes for GH deficiency in young children to elderly adults. An example of GH deficient children; are children who have growth issues and short stature also known as short height. Other more common causes for GH deficiency include genetic conditions and at birth malformations. GH deficiency can also cause dela sexual maturity because of the lack of androgens produced. People forget how important GH is for the production of hormones especially androgens. In adults, deficiency is rarely established; the most common cause is from a pituitary adenoma. Other causes of GH deficieny within adults include a continuation of a childhood problem, possibly due to formation of bodily form lesions or trauma, and in extremely rare cases they develop idiopathic GHD. Adults with GHD present with non-specific problems including obesity with a relative decrease in lean body mass and, and in most if not all cases, a severe drop in energy and overall quality of life. Diagnosis of GH deficiency is a detailed process that includes a multiple-step diagnostic examination, typically culminating in GH stimulation tests to see if the individual’s pituitary gland will release a GH pulse when aggravated by different variables\/stimuli.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBenefits of GH\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThere are a multitude of benefits with injecting GH. Had there been no benefits to it, no doctors would have been prescribing it for GHdeficiency. GH is known first and foremost through the bodybuilding community to build lean muscle tissue through sarcomere hyperplasia (splitting of muscle cells). GH also enhances lipolysis production which increases the rate in which fat is burned. GH triggers the growth of all organs except the brain. GH increases protein synthesis which will lead to more nitrogen retention giving you more muscle and more vascularity. GH protects the immune system by making it stronger to adapt to environmental changes. GH allows the bones of the body to retain calcium at higher rates which leads to a better bone density mineral state. GH is crucial for someone on a keto based diet as it promotes gluconeogenesis within the body’s Liver. Speaking of livers, it also reduces the uptake of nasty glucose within the Liver which reduces visceral adipose tissue located around the organs; this is very beneficial for Liver function. As anyone who knows a thing or two about the body, since the Liver coincides with the pancreas, GH is of benefit to the pancreas as well. GH is also needed for the production of hair, nails, teeth and even androgens. The more GH the body has, the more androgens the body will produce to go along the levels of GH throughout the body. In other words, GH is a must for the body to maintain homeostasis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eToo much of anything can pose a problem, although some bodybuilders may think differently. HGH can trigger side effects depending on the individual’s physiology, dosing, duration of use, and sensitivity. At higher doses of GH people can experience Joint inflammation which causes the Joint and muscle area to swollen.Joint pain is also common with GH therapy and usually comes about if inflammation of the Joint occurs. A no doubter is an increased risk of diabetes due to body’s lack of insulin sensitivity. Carpal tunnel syndrome can occur with GH therapy but is rare and is usually a worsening condition from the inflamed joints. Other side effects can include less sleep needed because of the frequent GH spike pulses which is why people on GH therapy will notice that they wake up three times a given night. Although with continuous use of GH this effect tends to go away. Other people will notice that GH in excess may make them sleep extremely deep and cause them to wake up groggy to the point that they want to continue sleeping. There has been documentation that the individual’s body became unresponsive to the GH treatment as defense mechanism due to the overflowing amount of GH that the individual was receiving. RARELY can GH cause acromegaly of a bone or organ if used at high dosages for a long period of time. Acromegaly is essentially an over growth of a bone or organ. People with heavyiness of the jaw or an increase in size of their digits or even head are people who suffer from this condition. Some other side effects that come with this condition include muscle weakness, excess sex hormone binding globulin production, acne, sweating, nerve pressure, and diabetes from lack of insulin sensitivity.The most common disease of GH excess is a pituitary gland tumor made from somatotroph cells of the front of the pituitary gland. The only times you see it in children are those who suffer from Gigantism or Pituitary Gigantism due to excessive GH production. These somatotroph adenomas are benign aka harmless and grow slowly, gradually producing more amounts of GH as time passes. Eventually, the adenoma may become large enough to cause headaches, impair vision and even induce blindness by pressure on the optic nerves, and even cause deficiency of other pituitary hormones such as androgens by displacement. This is why people need to take their GH injection in the early morning to avoid displacement of the body’s other hormones.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNow the fact that Fragement GH 176 only carries the benefits which as you see include protein synthesis, vascularity from increased nitrogen retention, increased bone mineral density, better sleep, and increased muscle mass through hyperplasia tells me it is worth every penny. This FRAGMENT of GH does not bring all the worries that regular GH can bring such hormone displacement, inflammation of the joints, weird sleeping patterns, and even acromegaly. The fact that its best attributes is increasing lipolysis tells us that this stuff works great on a cut, recomp and is ideal on a dirt bulk. It truly is a versatile peptide with lots of potential. Due to its lack of sides it is also can be used at higher dosages for quick boost in one’s goals with their GH abundance. I recommend that one start off with a daily dosage of 500mcg daily and work yourself up on dosing accordingly. Remember that studies confirm that this FRAGMENTstart to exhibit its pro lipolysis and fat oxidation effects at 500mcg’s. I am sure that once you starting implementing this FRAGMENT into your regime, you won’t want to stop using, and as with standard unrefined GH it gets better with continuous use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMolecular Formula : CC78H123N23O23S2 Molecular Weight : 1815.1 CAS No. : N\/A \u0026gt;99 % Purity\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSequence: Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFor RESEARCH PURPOSES ONLY.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn a study of Ng et al. (2000) on animal subjects, they found out that a 500mcg dosage of the said hormone increased the lipolytic activity in adipose tissues without having negative influence in the blood glucose level. Furthermore, though it behaves like a growth hormone , it does not causes hyperglycemia because it does not compete with GH receptors (Wu et al. 1993). Because of such effects, researchers have suggested that it might be used for the elimination of excess abdominal fat which is a significant aspect of HIV-associated lipodystrophy.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe HGH Fragment is a modified form of amino acids 176-191 at the C-terminal region of the human growth hormone (HGH). Studies have shown that it works by mimicking the way natural HGH regulates fat metabolism but without the adverse effects on insulin sensitivity (blood sugar) or cell proliferation (muscle growth) that is seen with unmodified HGH. Like unmodified GH, the HGH fragment 176-191 stimulates lipolysis (breaking down of fat) and inhibits lipogenesis (the formation of fatty acids and other lipids in the body).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH fragment 176-191 is estimated to be 12.5 times stronger than human growth hormone (HGH) for weight loss than standard human growth hormone (HGH).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOf particular note is that in studies HGH fragment 176-191 had the ability to increase muscle growth.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn most studies favorable results have been shown with dosages between 500-1000mcg or 5-10mcg\/kg split into multiple dosages per day. No adverse side effects were reported with continuous use per the dosage limits in the above example.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStudies have suggested the following:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA typical conservative protocol would be:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e250mcg in the morning plus\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e250mcg pre lunch plus\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e250mcg in the evening (pre-bed).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eApproximately 5-7 days a week – subcutaneous injections\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA more aggressive protocol would be:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e350mcg in the morning plus\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e350mcg 30 minutes prior to training\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e350mcg in the evening (pre-bed).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eApproximately 5-7 days a week – subcutaneous injections\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen dosing multiple times a day at least 3 hours should separate the administrations.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdministration should ideally be done on either an empty stomach or with only protein in the stomach. A diet high in protein is recommnded.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFragment 176-191 of HGH (Human Growth Hormone)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH Frag 176-191 is a stabilized analog of the factor, which stimulates Growth hormone secretion (somatoliberin). The scientists of the Monash University, Victoria, discovered that the GH effect of fat mass reduction is controlled by the small region near the end of GH molecule. This region consists of 176-191 amino acids, which is less than 10% of the total size of the GH molecule, and does not influence growth and insulin resistance.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTherefore, this drug has one single effect. It stimulates lipolysis (12.5 times stronger than GH) and significantly slows down lipogenesis (formation of fatty acids). Fragment 176-191 has neither other affects, nor side effects of the Growth hormone (for example, impaired control of blood glucose level). That is why this drug can be viewed to as an ideal drug for getting rid of excess fat. Some scientists declared that regular use of Fragment 176-191 could increase the level of IGF-1 and help to slow down aging processes.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMixing and our recommended dosage\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eYou inject 2ml water into the vial of HGH Frag 176-191 from the water vial. 1 full syringe is 1ml.You then wait for the vial powder content to dissolve ON ITS OWN. DO NOT SHAKE THE VIAL TO MIX POWDER. Once dissolved and clear in colour you draw out 0.2 on the syringe each morning, before breakfast and each night before bed, and inject it into the tummy under the skin into the fatty skin layer. It’s a total of 0.4 on the syringe per day taken in two lots, before breakfast and before bed. A vial should last 5 days.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741806682404,"sku":null,"price":870.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c6fb8615-5777-4ca0-b403-bc8f37d16739.jpg?v=1778055833"},{"product_id":"keifei-peg-mgf","title":"Keifei PEG MGF","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI MGF(PREGLYLATED MECHANO GROWTH FACTOR 2000MCG\/AMP =3 POWDER+WATER))\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePEG MGF is a splice variant of the IGF produced by a frame shift if the IGF gene and PEGylated to improve stability. PEG-MGF, or PEGylated Mechano Growth Factor, is a new and innovative form of the IGF produced by a frame shift if the IGF gene, namely Mechano Growth Factor (MGF), which is PEGylated to improve stability that outperforms natural MGF many times over. MGF is a splice variant of the IGF gene which increases stem cell count in the muscle and allows for muscle fibers to fuse and mature. This is a process required for growth of adult muscle. Natural MGF is made locally and does not travel into the bloodstream. Synthetic MGF is water based and when administered intramuscularly, travels into the bloodstream. MGF is only stable in the blood stream for only a few minutes. Research has shown that PEG-MGF helps increase the muscle stem cell count, so that more may fuse and become part of adult muscle cells. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePEGylation is the act of attaching a Polyethylene glycol (PEG) structure to another larger molecule (in this case, MGF). The PEG acts as a protective coating and the theory here is that this will allow the MGF to be carried through the blood stream without being broken down. Neurological research has shown that utilizing PEGylated MGF resulted in a longer more stable acting version of the MGF peptide in serum\/blood.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMechano Growth Factor (MGF) exhibits local effects in skeletal muscle and without cannot travel through the body without modification. The problem with synthetic Mechano Growth Factor (MGF) is that it is introduced intramuscularly and is water based so it goes into the blood stream. When used this way, Mechano Growth Factor (MGF) only remains stable in the blood stream for a few minutes. Biologically produced MGF is made locally and does not enter the bloodstream. It is also short acting so stability is not an issue. By PEGylating the Mechano Growth Factor (MGF) it is almost as efficient as local produced Mechano Growth Factor (MGF) when used intramuscularly. This is accomplished by surrounding part of the peptide with a structure of polyethylene glycol, which can be attached to a protein molecule. The polyethylene glycol groups protect the peptide but do not surround it completely. The active sites of the peptide are still free to do their biological function. In this case the shell is a negative charged shield against positively charged compounds that would affect the protein.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMechano Growth Factor (MGF): a local growth factor or a local tissue repair factor. MGF is derived from the insulin-like growth factor (IGF-1), but its sequence differs from the systemic IGF-1 produced by the liver. MGF is expressed as a form of IGF-1 by mechanically overloaded muscle when mechanical resistance is applied to muscles (such as weight training). At this point, the IGF-1 gene is spliced to produce IGF-1Ec (which is another name for MGF). It is expressed as a pulse following muscle damage and is apparently involved in the activation of muscle satellite cells[1]. This production of MGF can stimulate satellite cells into activation, to create new muscle fiber[2]. MGF also promotes nitrogen retention and new protein synthesis. It could actually be the case that this particular expression of MGF (IGF-1Ec) is an important part of the deciding factors in whether a muscle will grow or not. The introduction of this peptide, either by weight training or by an injection, will cause the affected area to respond by producing new muscle tissue. It would be safe to say that MGF presence in the muscle is one of the most major factors in the anabolic effect of resistance training (weight training). Currently, this compound is being used successfully by bodybuilders, for bringing up lagging body parts as well as overall growth.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMGF is being used successfully by bodybuilders, for bringing up lagging body parts as well as overall growth. The most relevant rodent data has been shown that MGF is a very potent inducer of muscle growth when it’s introduced into the muscle via an intramuscular injection of cDNA. In fact, in one study MGF caused a 20% increase in the weight of the injected muscle within 2 weeks[3]. Further investigation elucidated that this was actually due to an increase in the size of the muscle fibers.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMechanism\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMGF is extremely likely to cause myogenesis during skeletal muscle hypertrophy by contributing to at least by three important molecular processes: increased satellite cell activity, gene transcription and protein translation. Satellite cells in skeletal muscle provide the extra nuclei for postnatal growth[5] and that they are also involved in repair and regeneration following local injury of muscle fibers[6]. In normal adult undamaged tissue, the satellite cells are quiescent and usually detected just beneath the basal lamina. When activated, they commence to coexpress myogenic factors, including c-met, myoD, myf5, and, later, myogenin[7]. When introduced either by weight training or by an injection?MGF appears to stimulate satellite cells into activation. This in turn allows the activation of extra undamaged nuclei required for muscle fiber growth and repair to occur. In addition, the appearance of MGF initiates the upregulation of new protein synthesis. After this initial and short lived burst of splicing, IGF-1 production switches towards producing a systemic release of IGF-1Ea from the liver, which upregulates protein synthesis as well, but over a longer time line. During this process of regenerating muscle, myoblasts are formed to replace and hypercompensate for damaged\/destroyed ones, and then they can either fuse with each other to form totally new myofibers or become incorporated into previously damaged (surviving) myofibers. Ultimately, if more myofibers are created than were destroyed (by training) new muscle growth is experienced.  \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage and Administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt’s a good way for bodybuilders and other athletes to increase muscle weight by shooting MGF immediately post workout. At this point natural levels of MGF are already elevated. The addition of extra MGF should push more satellite cells towards the formation of new muscle tissue. Administration dosage of MGF should be at about 400mcgs\/day, which is injected into the primary muscle trained post workout – half going into that muscle on one side of the body, the other half going into the mirror image of that muscle on the other side. We suggest that a administration of IGF-1, such as IGF-1 Long R3, an hour after shooting of MGF will produce the additional activation of satellite cells, protein translation, and gene transcription. It will force the body to produce much more new tissue than if MGF or IGF are used at any other point during the day, or in a different sequence. It seems that MGF and IGF-1 appear to act synergistically and promote rapid new muscle growth.  \u003c\/div\u003e\n\u003cdiv\u003eDifferences between MGF, IGF-1 and HGH (human growth hormone)\u003c\/div\u003e\n\u003cdiv\u003eHGH is actually closely related to IGF-1, in a lot of ways. HGH, or GH in short, is certainly an effective fat burner and anabolic agent, and is a protein secreted by the pituitary. Once secreted, it has the ability to influence various cells in the body to increase in number and size, as well as having the ability to enhance the movement of amino acids through cell membranes- thereby increasing the rate at which the cells can convert those molecules to usable proteins. It also causes cells to preferentially burn fat in lieu of carbohydrates. The important thing to realize is that there is a mounting body of evidence that strongly suggests that these effects occur as a result of the IGF-1 released as a result of the pituitaries GH secretion. Scientists have discovered that many of HGH’s anabolic and regenerative effects are actually mediated by IGF-1. HGH indirectly causes muscle growth by stimulating the release of IGF-1 when it (the HGH) is destroyed in the human body. So one way you could look at it as HGH being a precursor to IGF-1. The later is more effective at directly causing muscle growth and density increases than HGH. Over the past few decades, HGH has developed quite a reputation for taking awhile (often several weeks) for the user to start seeing results. In contrast, IGF-1 often begins to product noticeable results within the first couple of weeks. With growth hormone you need to use high amounts of anabolics and often insulin to see any gains at all, this is not the case with IGF-1. IGF-1’s superiority to HGH is not only intuitive at some level, but has also been clearly elucidated clinically as well. In the following graphs taken from a rodent study comparing IGF-1 and HGH, a low dose as well as a high dose of IGF-1 was shown to be more anabolic than HGH. In comparison to HGH, IGF-1 produced an overall greater total protein content within the injected muscle as well as a greater final weight of the that muscle (called the “Tibialis Anterior” or TA)\u003c\/div\u003e\n\u003cdiv\u003eIt seems to be the case that IGF-1 would be superior to HGH as an anabolic agent. In some clinical studies, that is not always the case, but in most of bodybuilders and athletes, greater results are often seen with IGF-1 over HGH – and it should be noted that they are often seen more quickly as well.\u003c\/div\u003e\n\u003cdiv\u003eThe mature systemic type of IGF-1 is a simple 70 amino acid peptide, but its gene is unexpectedly large spanning a region of over 90 kb of genomic DNA. Alternative splicing of IGF-I gene results in different transcripts encoding several IGF-I precursor proteins. MGF is expressed by mechanically overloaded muscle and it is derived from the IGF-1, but its sequence differs from the systemic IGF-1 produced by the liver[9]. In addition to MGF expression being mechanosensitive, it has a unique carboxy peptide sequence . It was noted that in exon 5 there is an insert that changes the reading frame. In the rat it is 52 bases, but the human the insert is 49 bases. Amino acids are encoded by triplets of bases, and because the exon 5 sequence that is spliced into the MGF mRNA is not a multiple of 3, the downstream peptide sequence is different from that of the other IGF-1 isoforms. This has important functional consequences, because the carboxy peptide of some IGF-1 isoforms is involved in the recognition of the specific binding proteins that stabilize these growth factors. However, it appears that in the case of MGF the carboxy-terminal peptide (encoded by parts of exons 5 and 6) is unique and has now been shown to act as a separate growth\/repair factor from the IGF-1 receptor domain\u003c\/div\u003e\n\u003cdiv\u003eSplicing of the insulin-like growth factor (IGF) gene to produce different forms of IGF-I in human muscle. Mechano growth factor (MGF) is produced locally in response to exercise and it differs from the two systemic types of IGF-1 as the 49 base insert in the exon creates a reading frame shift so that the downstream or C-terminal peptide sequence is different. Reg Seqn, Regulatory sequence.\u003c\/div\u003e\n\u003cdiv\u003eAlthough MGF is a fairly new peptide, recent studies drawing the comparison between IGF-1 and MGF have concluded that MGF is even quicker to produce results. Actually, it’s been found in rodent studies to produce both faster and better results with regards to muscle growth, compared to IGF-1. It has been found by Goldspink G.’group that a single intramuscular injection of MGF cDNA into a mouse muscle resulted in a 25% increase in mean muscle fibre cross section area within three weeks. Similar experiments have been carried out using the systemic or liver type of IGF-1 in an adenoviral vector under the control of a muscle regulatory sequence. However, this took four months to produce a 15% increase and is probably due to the anabolic effect of IGF-1, which is common to all the splice variants. So far as we know, MGF is superior to IGF-1 and HGH for bodybuilders as an anabolic agent and this compound is being used successfully by bodybuilders, for bringing up lagging body parts as well as overall growth.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53741921468708,"sku":null,"price":850.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_f665763e-ff51-4b33-a322-7b685e2df6de.jpg?v=1778056006"},{"product_id":"keifei-growth-hormone-36iu-pen","title":"Keifei Growth Hormone 36iu Pen","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI MGF(PREGLYLATED MECHANO GROWTH FACTOR 2000MCG\/AMP =3 POWDER+WATER))\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePEG MGF is a splice variant of the IGF produced by a frame shift if the IGF gene and PEGylated to improve stability. PEG-MGF, or PEGylated Mechano Growth Factor, is a new and innovative form of the IGF produced by a frame shift if the IGF gene, namely Mechano Growth Factor (MGF), which is PEGylated to improve stability that outperforms natural MGF many times over. MGF is a splice variant of the IGF gene which increases stem cell count in the muscle and allows for muscle fibers to fuse and mature. This is a process required for growth of adult muscle. Natural MGF is made locally and does not travel into the bloodstream. Synthetic MGF is water based and when administered intramuscularly, travels into the bloodstream. MGF is only stable in the blood stream for only a few minutes. Research has shown that PEG-MGF helps increase the muscle stem cell count, so that more may fuse and become part of adult muscle cells. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePEGylation is the act of attaching a Polyethylene glycol (PEG) structure to another larger molecule (in this case, MGF). The PEG acts as a protective coating and the theory here is that this will allow the MGF to be carried through the blood stream without being broken down. Neurological research has shown that utilizing PEGylated MGF resulted in a longer more stable acting version of the MGF peptide in serum\/blood.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMechano Growth Factor (MGF) exhibits local effects in skeletal muscle and without cannot travel through the body without modification. The problem with synthetic Mechano Growth Factor (MGF) is that it is introduced intramuscularly and is water based so it goes into the blood stream. When used this way, Mechano Growth Factor (MGF) only remains stable in the blood stream for a few minutes. Biologically produced MGF is made locally and does not enter the bloodstream. It is also short acting so stability is not an issue. By PEGylating the Mechano Growth Factor (MGF) it is almost as efficient as local produced Mechano Growth Factor (MGF) when used intramuscularly. This is accomplished by surrounding part of the peptide with a structure of polyethylene glycol, which can be attached to a protein molecule. The polyethylene glycol groups protect the peptide but do not surround it completely. The active sites of the peptide are still free to do their biological function. In this case the shell is a negative charged shield against positively charged compounds that would affect the protein.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMechano Growth Factor (MGF): a local growth factor or a local tissue repair factor. MGF is derived from the insulin-like growth factor (IGF-1), but its sequence differs from the systemic IGF-1 produced by the liver. MGF is expressed as a form of IGF-1 by mechanically overloaded muscle when mechanical resistance is applied to muscles (such as weight training). At this point, the IGF-1 gene is spliced to produce IGF-1Ec (which is another name for MGF). It is expressed as a pulse following muscle damage and is apparently involved in the activation of muscle satellite cells[1]. This production of MGF can stimulate satellite cells into activation, to create new muscle fiber[2]. MGF also promotes nitrogen retention and new protein synthesis. It could actually be the case that this particular expression of MGF (IGF-1Ec) is an important part of the deciding factors in whether a muscle will grow or not. The introduction of this peptide, either by weight training or by an injection, will cause the affected area to respond by producing new muscle tissue. It would be safe to say that MGF presence in the muscle is one of the most major factors in the anabolic effect of resistance training (weight training). Currently, this compound is being used successfully by bodybuilders, for bringing up lagging body parts as well as overall growth.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMGF is being used successfully by bodybuilders, for bringing up lagging body parts as well as overall growth. The most relevant rodent data has been shown that MGF is a very potent inducer of muscle growth when it’s introduced into the muscle via an intramuscular injection of cDNA. In fact, in one study MGF caused a 20% increase in the weight of the injected muscle within 2 weeks[3]. Further investigation elucidated that this was actually due to an increase in the size of the muscle fibers.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMechanism\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMGF is extremely likely to cause myogenesis during skeletal muscle hypertrophy by contributing to at least by three important molecular processes: increased satellite cell activity, gene transcription and protein translation. Satellite cells in skeletal muscle provide the extra nuclei for postnatal growth[5] and that they are also involved in repair and regeneration following local injury of muscle fibers[6]. In normal adult undamaged tissue, the satellite cells are quiescent and usually detected just beneath the basal lamina. When activated, they commence to coexpress myogenic factors, including c-met, myoD, myf5, and, later, myogenin[7]. When introduced either by weight training or by an injection?MGF appears to stimulate satellite cells into activation. This in turn allows the activation of extra undamaged nuclei required for muscle fiber growth and repair to occur. In addition, the appearance of MGF initiates the upregulation of new protein synthesis. After this initial and short lived burst of splicing, IGF-1 production switches towards producing a systemic release of IGF-1Ea from the liver, which upregulates protein synthesis as well, but over a longer time line. During this process of regenerating muscle, myoblasts are formed to replace and hypercompensate for damaged\/destroyed ones, and then they can either fuse with each other to form totally new myofibers or become incorporated into previously damaged (surviving) myofibers. Ultimately, if more myofibers are created than were destroyed (by training) new muscle growth is experienced.  \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage and Administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt’s a good way for bodybuilders and other athletes to increase muscle weight by shooting MGF immediately post workout. At this point natural levels of MGF are already elevated. The addition of extra MGF should push more satellite cells towards the formation of new muscle tissue. Administration dosage of MGF should be at about 400mcgs\/day, which is injected into the primary muscle trained post workout – half going into that muscle on one side of the body, the other half going into the mirror image of that muscle on the other side. We suggest that a administration of IGF-1, such as IGF-1 Long R3, an hour after shooting of MGF will produce the additional activation of satellite cells, protein translation, and gene transcription. It will force the body to produce much more new tissue than if MGF or IGF are used at any other point during the day, or in a different sequence. It seems that MGF and IGF-1 appear to act synergistically and promote rapid new muscle growth.  \u003c\/div\u003e\n\u003cdiv\u003eDifferences between MGF, IGF-1 and HGH (human growth hormone)\u003c\/div\u003e\n\u003cdiv\u003eHGH is actually closely related to IGF-1, in a lot of ways. HGH, or GH in short, is certainly an effective fat burner and anabolic agent, and is a protein secreted by the pituitary. Once secreted, it has the ability to influence various cells in the body to increase in number and size, as well as having the ability to enhance the movement of amino acids through cell membranes- thereby increasing the rate at which the cells can convert those molecules to usable proteins. It also causes cells to preferentially burn fat in lieu of carbohydrates. The important thing to realize is that there is a mounting body of evidence that strongly suggests that these effects occur as a result of the IGF-1 released as a result of the pituitaries GH secretion. Scientists have discovered that many of HGH’s anabolic and regenerative effects are actually mediated by IGF-1. HGH indirectly causes muscle growth by stimulating the release of IGF-1 when it (the HGH) is destroyed in the human body. So one way you could look at it as HGH being a precursor to IGF-1. The later is more effective at directly causing muscle growth and density increases than HGH. Over the past few decades, HGH has developed quite a reputation for taking awhile (often several weeks) for the user to start seeing results. In contrast, IGF-1 often begins to product noticeable results within the first couple of weeks. With growth hormone you need to use high amounts of anabolics and often insulin to see any gains at all, this is not the case with IGF-1. IGF-1’s superiority to HGH is not only intuitive at some level, but has also been clearly elucidated clinically as well. In the following graphs taken from a rodent study comparing IGF-1 and HGH, a low dose as well as a high dose of IGF-1 was shown to be more anabolic than HGH. In comparison to HGH, IGF-1 produced an overall greater total protein content within the injected muscle as well as a greater final weight of the that muscle (called the “Tibialis Anterior” or TA)\u003c\/div\u003e\n\u003cdiv\u003eIt seems to be the case that IGF-1 would be superior to HGH as an anabolic agent. In some clinical studies, that is not always the case, but in most of bodybuilders and athletes, greater results are often seen with IGF-1 over HGH – and it should be noted that they are often seen more quickly as well.\u003c\/div\u003e\n\u003cdiv\u003eThe mature systemic type of IGF-1 is a simple 70 amino acid peptide, but its gene is unexpectedly large spanning a region of over 90 kb of genomic DNA. Alternative splicing of IGF-I gene results in different transcripts encoding several IGF-I precursor proteins. MGF is expressed by mechanically overloaded muscle and it is derived from the IGF-1, but its sequence differs from the systemic IGF-1 produced by the liver[9]. In addition to MGF expression being mechanosensitive, it has a unique carboxy peptide sequence . It was noted that in exon 5 there is an insert that changes the reading frame. In the rat it is 52 bases, but the human the insert is 49 bases. Amino acids are encoded by triplets of bases, and because the exon 5 sequence that is spliced into the MGF mRNA is not a multiple of 3, the downstream peptide sequence is different from that of the other IGF-1 isoforms. This has important functional consequences, because the carboxy peptide of some IGF-1 isoforms is involved in the recognition of the specific binding proteins that stabilize these growth factors. However, it appears that in the case of MGF the carboxy-terminal peptide (encoded by parts of exons 5 and 6) is unique and has now been shown to act as a separate growth\/repair factor from the IGF-1 receptor domain\u003c\/div\u003e\n\u003cdiv\u003eSplicing of the insulin-like growth factor (IGF) gene to produce different forms of IGF-I in human muscle. Mechano growth factor (MGF) is produced locally in response to exercise and it differs from the two systemic types of IGF-1 as the 49 base insert in the exon creates a reading frame shift so that the downstream or C-terminal peptide sequence is different. Reg Seqn, Regulatory sequence.\u003c\/div\u003e\n\u003cdiv\u003eAlthough MGF is a fairly new peptide, recent studies drawing the comparison between IGF-1 and MGF have concluded that MGF is even quicker to produce results. Actually, it’s been found in rodent studies to produce both faster and better results with regards to muscle growth, compared to IGF-1. It has been found by Goldspink G.’group that a single intramuscular injection of MGF cDNA into a mouse muscle resulted in a 25% increase in mean muscle fibre cross section area within three weeks. Similar experiments have been carried out using the systemic or liver type of IGF-1 in an adenoviral vector under the control of a muscle regulatory sequence. However, this took four months to produce a 15% increase and is probably due to the anabolic effect of IGF-1, which is common to all the splice variants. So far as we know, MGF is superior to IGF-1 and HGH for bodybuilders as an anabolic agent and this compound is being used successfully by bodybuilders, for bringing up lagging body parts as well as overall growth.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53742032584996,"sku":null,"price":1800.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_4ae28688-6ed1-4efd-8528-74c3f837ac2d.jpg?v=1778056110"},{"product_id":"keifei-primobolin-50-tabs-25mg","title":"Keifei Primobolin 50 Tabs 25mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cdiv\u003e\u003cspan\u003eKEIFEI PRIMABOL(25MG METHENOLONE ACETATE\/ TAB=50TABS)\u003c\/span\u003e\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 44-57\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 88\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 4-6 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic Steroid (Oral) OR (FOR INJECTION)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men-50-200-mg daily Women 50-100-mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Very low and only in very high dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eModerate Anabolic\/ Low Androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimobolan tablets are a moderately anabolic and low androgenic oral steroid that was reported as limited in use by most bodybuilders. This was likely simply because alone and when it was administered in listed dosages the drug was not very effective. However, gains were made in muscle mass and strength were consistently reported to be of a very high quality and were mostly retained post-cycle. Acetates are “said” to aid in fat burning, so this drug was mostly used in a stack pre-contest.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe problem in effectiveness lies in the fact that PRIMOBOLAN ACETATE is not a c17-ALFA-ALKYLATED steroid and is therefore mostly deactivated during the first pass through the liver. As the reader is aware, oral AAS are commonly altered to decrease liver deactivation. The most common alteration is called a c-17 alfa-alkylated drug. This alteration makes the liver work over-time to deactivate it and is therefore said to be highly liver toxic. (But so are most oral birth control drugs) But another alteration in structure allows Primobolan orals to be somewhat resistant to liver deactivation. It is referred to as unsaturation in the 1-position.This alteration allows the compound to resist metabolic deactivation by significantly shifting the 17-Keto redox potential toward creation of active 17-beta hydroxyl AAS. The result is an active oral AAS that is not liver toxic except in very high dosages.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome have recalled the injectable form of Primobolan acetate with great fondness for its supposed fat burning\/lean mass building qualities. The vials contained only 20-mg\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eof METHENOLONE ACETATE (MA) yet it was reported far more effective than 150-\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003emg of the oral. A commonly reported method to obtain greater blood circulatory levels of the oral form was to mix 20-25-mg of the ground tables with either DMSO gel or a 50\/50 solution of DMSO and water. Users then simply applied the mixture to their skin (especially in areas of stubborn fat deposits). 10-20% absorbed and passed directly into the blood stream thus avoiding first pass liver deactivation. This was done 1-5 times daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDMSO is a solvent that carries smaller molecule structures mixed with it directly through the skin. It is said to be found at some health food stores and chemical supply warehouses.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnother reported method was mixing ground Primobolan tabs with Vitamin-E oil. The users then ingested it orally. This caused a great deal of the active steroid to be absorbed through the lymph system like Andriol and therefore avoid first pass deactivation.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*There is a great deal of research under way in the OTC supplement industry that employs a similar pharmacological solution to liver destruction of micronutrients.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBack to reported tablet use…\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimobolan tabs were reportedly used most by women and steroid novices because they do not aromatize or cause water retention. Women who utilized 50-100mg daily of this drug seldom noted virilizing side effects. Most report a distinct harder look and a 3-4 LB muscle mass gain in 6-8 weeks. Obviously many females also stacked Primobolan tabs with other drugs to heighten results. Males normally ingested 100-200 mg daily in 2-4 divided doses (due to short half-life 4-6 daily divided dosages were more effective at maintaining plasma concentrations of the active drug) and report fair gains. Stacked with more androgenic steroids such as testosterone, Parabolan, or even moderate androgenics such as Deca Durabolin or Equipoise, males made high quality muscle mass and strength gains with safer low side effect results.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Since Primobolan is a derivative of dihydrotestosterone (DHT) an acceleration in hair loss can occur in those with genetic receding hair lines (but was rarely noted).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimabolin is indicated in the treatment of refractory deficient red cell production anemias. These may include aplastic anemia, myelofibrosis, myelosclerosis, agnogenic myeloid metaplasia, and hypoplastic anemias caused by malignancy or myelotoxic drugs.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimabolin is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimabolin (Methenolone Acetate) has been used in certain countries to counteract catabolic states, for example after major trauma\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53742099857700,"sku":null,"price":1030.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_e5b4e5c4-ed63-463b-968b-eeaeb720d8bf.jpg?v=1778056211"},{"product_id":"keifei-winstrol-inject-50-20ml","title":"Keifei Winstrol Inject 50 20ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eKEIFEI WINSTROLBOLIN 50(50MG\/ML STANOZOLOL=20ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eINJECTABLE VERSION\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 30\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 320\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD METHYLTESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 48 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: High Anabolic\/Androgenic steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 50-100mg every 1-2 days Women 25-50-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Rare from real Stanozolol\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes, moderate when injected\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: None, DHT variant\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: No, DHT derivative (Potential for DHT receptor stimulation)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe injection form of stanozolol is a water based injectable steroid that is a derivative of DHT. Both oral and injectable forms are c17-alfa-alkylated chemicals. This of course makes the injectable form moderately liver toxic and the oral form liver toxic in high dosages. Before going on let me make it clear that the injectable form is the same as the oral. For this reason the injectable form has frequently been used as an oral also. Why would anyone have done that? Well, all c17-alfa-alkylated AAS, when passing through the liver for deactivation, cause a distinct elevation in IGF-1 production. (*Please see IGF-1). This is why 30-mg of Dianabol orals daily (210-mg weekly total) has been revered as more effective for mass and strength gains than 400-mg of testosterone enanthate. The injectable stanozolol has been much cheaper than oral stanozolol, so some athletes opted to utilize it as an oral.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is a high anabolic \/moderate androgenic that causes a significant elevation in protein synthesis and an improved nitrogen retention. Since it does not aromatize to estrogen, water retention, gyno, and female pattern fat deposits do not occur. A high protein diet of 1.5-2-g of protein per LB of bodyweight daily was necessary to obtain the best results. This was not noted as a steroid for rapid weight gains but was commonly affirmed as ideal for a continuous slow gain in very high quality lean muscle mass that was well retained after discontinuance. Many who compete utilized Winstrol off-season with testosterone in a Max Androgen Phase for its anabolic value.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMany used Winstrol (stanozolol) as a pre-contest drug because it provided a continuously harder appearance. When 50-100mg every 1-2 days was stacked with 76-mg of Parabolan every 2-3 days, the results were quite impressive. Many also added Masteron, Equipoise, or Testosterone Propionate\/ Testosterone Suspension with the addition of anti-estrogens for water retention and aromatization control.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen often reported use of Winstrol Depot. “Usually” those who reported 25mg 2-3 times weekly or a single weekly 50-mg injection use reported no virilization effects. (I have known many women who have utilized 50-100mg daily of this drug) Stacked with Oxandrolone and\/or Durabolin, women achieved excellent quality lean mass gains.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWinstrol tabs were often thought to be a better choice at a dosage of 10-20-mg daily, or about 1\/4 -1\/2ml of the injectable taken orally due to results realized. The method often employed for the injection product used as an oral was to mix 1ml of Stanozolol with 9 ml of water. Each ml=5-mg. (Duh!)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSince Stanozolol produced a surprising increase in strength, it has been used as a part of a mass cycle as well. Novices and older males made very impressive “second cycle” gains stacking 50mg of Stanozolol every other day with 50-100mg of Primobolan Depot every 2-3 days, or with 200-400mg of Deca-Durabolin weekly. Many hard-core males reported serious strength and mass gains using 50-100mg stanozolol with 50-100mg Testosterone Suspension daily. This was a fairly high weekly dosage and was hopefully considered for advanced athletes..if at all.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWinstrol is another AAS that was commonly used in a site-injection protocol for lagging body parts.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*I have been impressed with the results I have seen, but this method requires careful location. Hitting a vein would end any Mr. “O” dream real quick. Some black market Winstrol is testosterone suspension, so if gyno was reported…\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53742157070628,"sku":null,"price":650.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_009a0e6a-a390-4d78-a681-6cb65b1e45d6.jpg?v=1778056337"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/collections\/rn-image_picker_lib_temp_ef15da94-6b5e-407d-961b-6413d2e202bd.jpg?v=1777554680","url":"https:\/\/ultrafizique.co.za\/collections\/keifei.oembed?page=2","provider":"UltraFizique","version":"1.0","type":"link"}