PEG-MGFGrowth Factor Analog PeptideSafety Rating 6/10

TypePEGylated MGF (extended half-life)
CASNot standardized
MWMGF core ≈2,867 g/mol + PEG (variable)
AAs24 (peptide core)
Primary research areaMuscle / IGF research

Research-literature reference data, NOT patient instructions. Not for human use. Consult a licensed clinician for any human application.

Research dose rangeLimited clinical data; research protocols 200–400 mcg 2–3x/weeksource ↗
AdministrationSubcutaneous injection
Half-lifeSeveral days (pegylated)
Safety6/10 · Not FDA-approved
NCAA D1Banned

Price Comparison

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9 vendors competing

VendorPrice$ / mgUpdated
Core PeptidesBest $/mgCOA ✓ · 3P$63.00$12.60Apr 16, 2026Buy →
BioLongevity LabsCOA ✓ · 3P$94.97$18.99Apr 16, 2026Buy →
Modern AminosCOA ✓ · 3P$38.00$19.00May 14, 2026Buy →
Behemoth LabzCOA ✓ · 3P$194.42$19.44May 14, 2026Buy →
Guru PeptidesCOA unknown$38.99$19.50May 16, 2026Buy →

Overview

About PEG-MGF

Mechanism of action

PEGylated analogue of mechano growth factor (MGF, splice variant of IGF-1); activates satellite cells for muscle repair; promotes myoblast proliferation; PEGylation extends half-life dramatically.

Safety profile

Hypoglycemia risk, water retention, potential insulin resistance, injection site reactions. Similar IGF-1 axis risks. · PEGylated MGF; extended half-life; limited data; no proven major harms; sourcing quality main concern

Storage

Stability & handling

❄️Lyophilized (powder)−20°Clong-term stable
💉Reconstituted2–8°Cwithin 30 days
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Research

Studies & key findings

  • PEGylation of the MGF E-domain peptide extends its half-life by creating a hydrophilic polymer shield that reduces renal clearance and protease degradation, converting a peptide that degrades in minutes into one with a half-life measured in hours — enabling systemic rather than purely local delivery.
  • A sheep model of myocardial infarction found that intravenous administration of the MGF E-domain reduced the area of compromised cardiac muscle by 35% compared to controls and preserved systolic function, suggesting that when delivered systemically at sufficient concentrations the peptide reaches ischemic tissue and is cardioprotective.

6 peer-reviewed sources cited — clinical, preclinical, and regulatory.

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