GLOW Blend
Stylized molecular signature · scaled by MW
Variable across the three components — characterize each independently: GHK-Cu ~30–60 min (rat, SC), BPC-157 ~15 min (rat, IV), TB-500/Tβ4 ~1.5–3 h (human IV; dose-dependent).
This is a multi-component blend; the value above is the dominant component, not the formulation total.
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How it’s studied.
A multi-peptide blend combining GHK-Cu (70 mg) for ECM remodeling and copper-mediated antioxidant gene expression, BPC-157 (10 mg) for proposed angiogenesis-modulating tissue-repair signaling, and TB-500 analog (10 mg) for actin-sequestration and cell-migration activity. In research literature, these components are individually studied and their combined behavior is an active research interest in systemic tissue-repair models.
GLOW Blend is a Peptide Plus formulation combining three peptides studied independently for tissue-repair pathways. The listed molecular weight reflects the GHK-Cu component only and is used as a sort key — a single MW is not meaningful for a multi-peptide blend. Reconstitution and dose calculations should be performed per-component using each peptide's mass within the blend (the calculator on this site can be re-run for each component).
- 01
Combined tissue-repair research
- 02
Multi-pathway healing studies
- 03
Systemic inflammation research
Per-component reconstitution; verify each peptide's literature dose range independently.
Verify each value in primary literature.
Pre-filled defaults for GLOW Blend.
- Concentration
- 2.50mg/mL
- Draw on U-100
- 10units
- Volume / dose
- 0.100mL
- Doses / vial
- 20
Assumes 27-gauge insulin syringe, U-100 markings. Verify before use.
Open in calculatorCo-factors and supporting compounds.
Sparse literatureCompounds identified in published research as sharing pathways with GLOW Blend, or studied alongside it in trials. Reference material only — not a recommendation, not medical advice. Citations link to PubMed.
GLOW Blend is a multi-peptide formulation combining GHK-Cu, BPC-157, and TB-500. No published PubMed literature studies this exact blend or characterises cofactors specific to the combination. Co-factor data for this blend should follow the component peptides — see the ghk-cu, bpc-157, and tb-500 entries in this report. The cross-cutting cofactors that appear in multiple component entries (ascorbate for the collagen hydroxylation step, zinc as a permissive cofactor for MMP-mediated matrix remodelling, and the copper-zinc balance caution from the GHK-Cu entry) are the most defensible carry-overs for any GLOW-Blend protocol-design discussion.