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For in vitro laboratory research use only/Not for human or veterinary use
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GLOW 70mg

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GLOW

70mg · Single vial · Lyophilized powder

Single vial85.99CAD

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Sender: Vennori Biosciences · orders@vennori.com

Dose
70mg
Pack size
Single vial
Form
Lyophilized powder
Storage
2–8°C

In vitro laboratory research use only · Not for human or veterinary use · Batch documented · Third-party tested · Ships from Canada

§ Verification — Batch 2026-05

Certivos verified

Janoshik Analytical

Independent Analysis

Test date
2026-06-11

Certificates are issued and hosted by Certivos.

§ Research

Research · BPC + GHK-Cu + TB-500

Overview

BPC + GHK-Cu + TB-500 is a research combination of three independently studied compounds. BPC-157 is a synthetic 15-residue sequence derived from a protein fraction originally isolated from human gastric juice. GHK-Cu is the copper(II) complex of the endogenous Gly-His-Lys sequence, first identified in human plasma. TB-500 is a synthetic analog derived from thymosin beta-4, a 43-residue actin-sequestering protein expressed in most nucleated cells, and is commonly described as incorporating its actin-binding region. The blend is supplied for laboratory investigation of tissue-repair, angiogenesis, and cell-migration pathways.

Mechanism of action

Each component acts through a distinct pathway. BPC-157 has been reported to interact with the nitric oxide system and to modulate VEGFR2 expression and FAK-paxillin signaling in endothelial and fibroblast models. GHK-Cu binds copper(II) with high affinity and is proposed to act as a copper-delivery and signaling complex, with gene-expression analyses indicating modulation of transcripts governing extracellular matrix synthesis and remodeling. Thymosin beta-4 sequesters monomeric G-actin, regulating cytoskeletal dynamics and cell motility, and has been shown to form a complex with PINCH and integrin-linked kinase, activating Akt survival signaling in cardiac and endothelial cells.

Key research findings

  1. 01

    Preclinical rodent studies of BPC-157 characterize effects on angiogenesis, vascular collateral recruitment, and tissue-repair endpoints in gastrointestinal, tendon, and vascular injury models.

  2. 02

    In vitro and gene-expression studies of GHK-Cu document modulation of collagen and glycosaminoglycan synthesis and broad shifts in transcript profiles in human cell lines.

  3. 03

    Murine myocardial infarction studies of thymosin beta-4 (2004) characterized integrin-linked kinase activation, cardiomyocyte migration and survival, and effects on cardiac function endpoints.

  4. 04

    The combination itself has not been characterized as a single entity in peer-reviewed studies; available data derive from investigations of each component individually.

Published references

  • BPC 157 and blood vessels

    Seiwerth S et al. — Curr Pharm Des, 2014 · PMID: 23782145

  • GHK and DNA: resetting the human genome to health

    Pickart L et al. — Biomed Res Int, 2014 · PMID: 25302294

  • Thymosin beta4 activates integrin-linked kinase and promotes cardiac cell migration, survival and cardiac repair

    Bock-Marquette I et al. — Nature, 2004 · PMID: 15565145

The information above is derived from published preclinical and clinical research. It is provided for educational purposes only and does not constitute medical advice, diagnosis, or treatment recommendations.