GDF-8 1mg
Growth Differentiation Factor 8 (Myostatin)
Mature myostatin: 109 amino acid homodimer
Overview
GDF-8, commonly known as myostatin, is a member of the TGF-beta superfamily that serves as the primary negative regulator of skeletal muscle growth. It was discovered by Se-Jin Lee and Alexandra McPherron at Johns Hopkins University in 1997 when they created myostatin knockout mice that developed dramatically increased muscle mass (approximately 2-3 times normal). Myostatin signals through activin type IIB receptors (ActRIIB) on muscle cell surfaces, activating the SMAD2/3 transcription factor pathway. This signaling inhibits myoblast proliferation and differentiation, suppresses protein synthesis via mTOR pathway inhibition, and promotes protein degradation through the ubiquitin-proteasome system. The net effect is powerful suppression of muscle growth and maintenance. Research-grade GDF-8 is used as a tool compound to study myostatin signaling pathways, develop myostatin inhibitors, and understand muscle wasting conditions. Natural mutations that reduce myostatin function have been identified in cattle (Belgian Blue, Piedmontese), dogs (whippets), sheep, and at least one documented human case — all resulting in exceptional musculature. This genetic validation has made myostatin inhibition a major therapeutic target for muscle wasting diseases including muscular dystrophy, sarcopenia, and cancer cachexia.
Mechanism of Action
GDF-8, commonly known as myostatin, is a member of the TGF-beta superfamily that serves as the primary negative regulator of skeletal muscle growth. It was discovered by Se-Jin Lee and Alexandra McPherron at Johns Hopkins University in 1997 when they created myostatin knockout mice that developed dramatically increased muscle mass (approximately 2-3 times normal). Myostatin signals through activin type IIB receptors (ActRIIB) on muscle cell surfaces, activating the SMAD2/3 transcription factor pathway. This signaling inhibits myoblast proliferation and differentiation, suppresses protein synthesis via mTOR pathway inhibition, and promotes protein degradation through the ubiquitin-proteasome system. The net effect is powerful suppression of muscle growth and maintenance. Research-grade GDF-8 is used as a tool compound to study myostatin signaling pathways, develop myostatin inhibitors, and understand muscle wasting conditions. Natural mutations that reduce myostatin function have been identified in cattle (Belgian Blue, Piedmontese), dogs (whippets), sheep, and at least one documented human case — all resulting in exceptional musculature. This genetic validation has made myostatin inhibition a major therapeutic target for muscle wasting diseases including muscular dystrophy, sarcopenia, and cancer cachexia.
Key Research Findings
- McPherron et al. (1997) discovered myostatin and showed that myostatin-null mice develop approximately 2-3x normal muscle mass, establishing myostatin as the key negative regulator of muscle growth.
- Lee & McPherron (2001) demonstrated that myostatin inhibition (via follistatin or dominant-negative ActRIIB) increases muscle mass even in wild-type adult mice.
- Schuelke et al. (2004) reported the first human case of a myostatin loss-of-function mutation, in an infant with remarkable muscle hypertrophy at birth.
- Elkina et al. (2011) reviewed the role of myostatin signaling in muscle wasting conditions and the therapeutic potential of myostatin inhibition.
Citations & References
Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member
McPherron AC, Lawler AM, Lee SJ. — Nature (1997)
Regulation of myostatin activity and muscle growth
Lee SJ, McPherron AC. — Proc Natl Acad Sci USA (2001)
Myostatin mutation associated with gross muscle hypertrophy in a child
Schuelke M, Wagner KR, Stolz LE, et al. — N Engl J Med (2004)
Dosage in Research
Used as a signaling tool compound at 10-100 ng/mL in cell culture. In vivo dosing varies by application. Recombinant myostatin is typically used for signaling studies rather than direct administration protocols.
Dosage information is derived from published research literature and is presented for educational purposes only. This is not medical advice. All products are for laboratory research use only.
Storage & Handling
Store lyophilized (freeze-dried) powder at -20°C to 4°C in a dry environment protected from light. Unreconstituted peptide is stable for extended periods when stored properly.
Once reconstituted with bacteriostatic water or an appropriate solvent, store at 2-8°C and use within the timeframe specified on the Certificate of Analysis. Avoid repeated freeze-thaw cycles.
A Certificate of Analysis documenting purity, identity, and recommended storage conditions is included with every order.
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Research Use Only
All products are intended for laboratory research and educational purposes only. Products have not been evaluated by the FDA and are not intended for human consumption, diagnosis, treatment, or prevention of any disease. Purchasers must be 21+ and confirm research use intent.