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Factory Supplying Peptide Lyophilized Powder Peg MGF (5mg)

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Factory Supplying Peptide Lyophilized Powder Peg MGF (5mg)
 
MGF Basic Info.:
 
Product Name: MGF ( Mechano Growth Factor )
Synonyms: MGF;Anti-STAT5A, C-Terminal antibody produced in rabbit;Mammary gland factor;STA5A;Anti-STAT5A antibody produced in rabbit;STAT5, His tagged human;STAT5A
CAS No.: N/A
Molecular Formula : C121H200N42O39
Molecular Weight : 2867.2
Storage temp.: -20°C
Form: lyophilized powder
Sequence: Tyr-Gln-Pro-Pro-Ser-Thr-Asn-Lys-Asn-Thr-Lys-Ser-Gln- Arg-Arg-Lys-Gly-Ser-Thr-Phe-Glu-Glu-Arg-Lys-NH2
Packing: 5mg/vial
 
MGF Description:
 
PEGylation 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.
 
MGF Application:
 
Using PEG MGF on cycle or off cycle, you are going to experience recovery that is far superior to any generic peptide available. Just like normal peptides, remember that PEG MGF comes in the form of a white delicate powder that needs to be reconstituted with bacteriostatic water and kept in the refrigerator.
 
PEG MGF Dosage:
 
Typical dosage of PEG-MGF is between 200mcg. - 400mcg. per week but many bodybuilders have said to "research" this peptide at dosages exceeding 1,500 mcg weekly with no adverse effects.
Because PEG MGF can cause site specific muscle growth, it is recommended to inject PEG MGF bi-laterally to ensure symmetrical gains. The most effective test results were experienced in users injecting the PEG MGF post exercise.
 

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Dehydroisoandrosterone (DHEA) (Steroids) 
 
Basic Info.
Synonyms: 3beta-Hydroxy-5-androsten-17-one; Dehydroepiandrosterone; trans-Dehydroandrosterone; Prasterone; Hydroxyandrostenone; Dehydroepian drosterone; 
Model NO.:CAS: 53-43-0                                                    Assay: 99.8% min.  
MF: C19H28O2                                                                   MW: 288.43 
Export Markets:Global
 
Additional Info.
Trademark:great-steroids                           Packing:foil bag or tin.
Standard: Enterprise standard                                              Origin:China
Melting point: 149℃~151℃                                                 Loss on dry: ≤0.5%
EINECS: 200-175-5                                                             Delivery: Express courier.
Character: White crystalline powder. Melting point 149-151 °C. Soluble in benzene, ethanol, ethyl ether, insoluble in chloroform, petroleum ether
Usage: pharmaceutical intermediates, For the production of steroidal hormone drugs and contraceptives, the main raw material. Downstream products acetylene progesterone.
 
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High Purity Gw-501516 GW501516 For Weight Loss 317318-70-0

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High Purity Gw-501516 GW501516 For Weight Loss 317318-70-0
 
GW 501516 Basic Info:
 
Product Name: GW501516
Alias: Cardarine
CAS No.: 317318-70-0
Molecular Formula: C21H18F3NO3S2
Molecular Weight: 453.50
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Powder
Usage: Fat loss
Dose: The recommended dosage for GW is 10-20 mg and for 8 weeks length
 
GW 501516 Description:
 
GW501516 is the name of a Glaxo Wellcome drug (the GW stands for the company and the number
is that of the product). It is also known as GW-501,516, GW1516, GSK-516).
 
GW-501516 is a selective agonist with high affinity and it is very potent. Various studies on this
PPAR receptor in lab rats indicates that it regulates the various proteins that the body uses for
energy. Rats with high fat and low metabolism were given the product and they were able to
lose weight and to increase overall energy levels.
 
GW 501516 Application:
 
GW501516 (also known as GW-501,516, GW1516, GSK-516 and on the black market as Endurobol) is a PPARδ receptor agonist that was invented in a collaboration between Ligand Pharmaceuticals and GlaxoSmithKline in the 1990s, was entered into clinical development as a drug candidate for metabolic diseases and cardiovascular diseases, and was abandoned in 2007 because animal testing showed that the drug caused cancer to develop rapidly in several organs.
 
In 2007 research was published showing that high doses of GW501516 given to mice dramatically improved their physical performance; the work was widely discussed in popular media, and led to a black market for the drug candidate and to its abuse by athletes as a doping agent. The World Anti-Doping Agency (WADA) developed a test for GW501516 and other related chemicals and added them to the prohibited list in 2009; it has issued additional warnings to athletes that GW501516 is not safe.
 
History Of GW 501516:
 
Concerns were raised prior to the 2008 Beijing Olympics that GW501516 could be used by athletes as an ergogenic performance-enhancing drug that was not currently controlled by regulations or detected by standard tests. One of the main researchers from the study on enhanced endurance consequently developed a urine test to detect the drug, and made it available to the International Olympic Committee. The World Anti-Doping Agency (WADA) developed a test for GW501516 and other related PPARδ modulators,and added such drugs to the prohibited list in 2009.
 
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N-(2-Methyl-5-nitrophenyl)-4-(pyridin-3-yl)pyrimidin-2-amine is used as a pharmaceutical intermediate.

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Product Description:
CAS: 831217-01-7                     Assay: 99%                   
M. F.: C25H34N6O3                    M. W.: 466.583  
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