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Muscle Building Peptides GDF-8 for Bodybuilding

CATEGORÍA Y ETIQUETAS:
Péptidos
Número de modelo: GDF-8
Certificación: YO ASI 9001, USP,GMP
Lugar de origen: porcelana
Cantidad mínima de pedido: 10gramo
Precio: Estanozolol semielaborado de la serie líquida de esteroides
Términos de pago: Western Union,Pago de Pequeña Cantidad ,Bitcoin, T / T
Capacidad de suministro: 5000kg/mes
El tiempo de entrega: 3-5 dias laborables
detalles del empaque: Paquete bien disfrazado ; Foil bag 25kg/drum; 1kg/bolsa de aluminio
Nombre del producto: GDF-8
Adecuado para: Adulto
consulta
  • Especificaciones

Muscle Building Peptides GDF-8 for Bodybuilding

Detalle rápido :

Nombre del producto: GDF-8 (Growth Differentiation Factor 8 miostatina)
Pureza: 85%
Especificación: 1mg
Almacenamiento:2-8 degree centigrade refrigerator
Paquete: 10 Vials/Kit
Deliver:1 working day for ready goods,7 days to your destination.
Pacakge:1kit=10vials Alumnium foil+bubble+carton
personalizado:accepted.
Country of Origin: porcelana

Descripción

Growth and differentiation factor 8 (GDF-8) (also known as muscle growth inhibin) is a muscle cell that produces and releases proteins from muscle cells that act on the autocrine function of muscle cells to inhibit myocyte production: muscle cell growth And differentiation. In humans, it is encoded by the MSTN gene. Myosin is a secreted growth factor that is a member of the TGF beta family of proteins.

Animals lacking myostatin or substances treated with substances that block myostatin activity have significantly more muscle mass. Además, individuals with mutations in the two copies of the myostatin gene have significantly more muscle mass and are stronger than normal. Blocking the activity of myostatin may have a therapeutic effect in the treatment of muscle wasting diseases such as muscular dystrophy.

Solicitud

1) The gene encoding myostatin was discovered in 1997 by geneticists Se-Jin Lee and Alexandra McPherron who produced a strain of mutant mice that lack the gene. These myostatinknockoutmice have approximately twice as much muscle as normal mice. These mice were subsequently namedmighty mice”.

2) Naturally occurring deficiencies of myostatin have been identified in cattle by Ravi Kambadur, whippets, y humanos; in each case the result is a dramatic increase in muscle mass. A mutation in the 3UTR of the myostatin gene in Texel sheep creates target sites for the microRNAs miR-1 and miR-206. This is likely to cause the muscular phenotype of this breed of sheep.

3) Human myostatin consists of two identical subunits, each consisting of 109 (NCBI database claims human myostatin is 375 residues long) amino acid residues. Its total molecular weight is 25.0 kDa. The protein is inactive until a protease cleaves the NH2-terminal, recetas de cocina “pro-domainportion of the molecule, resulting in the active COOH-terminal dimer. Myostatin binds to the activin type II receptor, resulting in a recruitment of either coreceptor Alk-3 or Alk-4. This coreceptor then initiates a cell signaling cascade in the muscle, which includes the activation of transcription factors in the SMAD familySMAD2 and SMAD3. These factors then induce myostatin-specific gene regulation. When applied to myoblasts, myostatin inhibits their differentiation into mature muscle fibers.

Myostatin also inhibits Akt, a kinase that is sufficient to cause muscle hypertrophy, in part through the activation of protein synthesis. Sin embargo, Akt is not responsible for all of the observed muscle hyperthrophic effects which are mediated by myostatin inhibition[8] Thus myostatin acts in two ways: by inhibiting muscle differentiation, and by inhibiting Akt-induced protein synthesis.

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