Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
Muscle / Myostatin
Also known as: FST Β· FST-344
A myostatin-pathway protein discussed for muscle growth. Human evidence is essentially absent for research-market use.
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Follistatin binds and inhibits myostatin and related factors.
Largely experimental (gene-therapy research); research-market peptide use is unvalidated.
Manipulating the myostatin pathway has unknown long-term human risks; unverified material.
Not an approved medicine. Research/experimental status.
Vendor comparison
The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
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Follistatin binds and inhibits myostatin and related factors.
Follistatin (also written FST, with the FST-344 isoform frequently referenced) is a naturally occurring glycoprotein best known for its role in the myostatin signalling pathway. Myostatin is a member of the TGF-beta superfamily that acts as a brake on skeletal muscle growth; follistatin binds and inhibits myostatin along with several related growth factors, and by neutralising that brake it is theorised to permit increased muscle mass. This mechanism is why follistatin appears so often in discussions of muscle growth, body composition, and "myostatin inhibition." On peptides.cx it is catalogued in the Muscle / Myostatin category as an educational reference entry, not as a product recommendation or a guide to use.
It is important to be honest about where the evidence actually stands. The strongest follistatin data comes from animal models, where boosting follistatin activity or suppressing myostatin produces marked increases in muscle size, and from experimental gene-therapy research in which a follistatin gene is delivered to tissue. Human evidence for follistatin as an injectable research-market peptide is essentially absent: the controlled human work that exists sits in the gene-therapy and clinical-research world, not in the loose "research peptide" market, and those are very different things. That gap matters. A vial sold as "follistatin" is unverified material of unknown identity, purity, and biological activity, and none of the aspirational muscle-growth claims attached to it have been validated in humans in that context.
Follistatin is not an approved medicine and holds a research or experimental status only. Because it manipulates a core growth-regulatory pathway, its long-term effects in humans are genuinely unknown, and deliberately altering the myostatin axis carries risks that have not been characterised. This page summarises what follistatin is, why researchers study it, and the current evidence and safety picture so readers can understand the science accurately. It is educational reference content and does not provide medical advice, dosing, protocols, or sourcing guidance.
Evidence grade: D
Largely experimental (gene-therapy research); research-market peptide use is unvalidated. Muscle-growth effects in models.
Largely experimental (gene-therapy research); research-market peptide use is unvalidated.
Muscle-growth effects in models.
Manipulating the myostatin pathway has unknown long-term human risks; unverified material.
Not an approved medicine. Research/experimental status.
Late 1980s
Follistatin is first isolated from ovarian follicular fluid and named for its ability to suppress follicle-stimulating hormone (FSH), initially studied as a reproductive-endocrine protein.
1990s
Research establishes follistatin as a binding protein for activin and, following the discovery of myostatin as a negative regulator of muscle mass, it is identified as an inhibitor of the myostatin pathway.
2000s
Preclinical animal studies report substantial muscle-growth effects when follistatin is over-expressed or delivered, driving interest in the myostatin pathway as a target for muscle-wasting conditions.
Early 2010s
Gene-therapy approaches using viral vectors to deliver the follistatin (FST-344) gene are tested in early-phase human trials for muscular dystrophies and inclusion-body myositis, the main context in which follistatin has been studied in people.
Early 2020s
Follistatin appears on the research-chemical and 'research peptide' market marketed toward muscle growth, despite no approval and essentially no validated human evidence for this form of use.
2020s (ongoing)
Follistatin remains an unapproved, experimental compound; regulated development stays confined to gene-therapy research rather than injectable research-peptide products.