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10mg BPC-157 + 50mg GHK-Cu + 10mg TB-500 (GLOW) – 70mg

$130.00

GLOW is a proprietary multi-peptide research blend composed of GHK-Cu (60MG), BPC-157 (15MG), and TB-500 (15MG), formulated for synergistic in vitro and in vivo study of cellular signaling, tissue regeneration, angiogenesis, and peptide-receptor interactions. This product is supplied as a lyophilized powder and is intended strictly for research purposes only.

278 in stock

Description

Research Overview


This blend combines three distinct peptides with well-characterized research profiles:

  • GHK-Cu (Copper Tripeptide): A naturally occurring copper-binding peptide involved in gene expressiontissue remodeling, and anti-inflammatory signaling
  • BPC-157: A synthetic peptide fragment derived from body protection compound, studied for its influence on angiogenesiscell migration, and cytokine activity
  • TB-500 (Thymosin Beta-4 Fragment): A synthetic version of a naturally occurring actin-sequestering peptide, associated with cell migrationwound modeling, and vascular modulation
The specific ratio of this formulation (GHK-Cu 50%, BPC-157 5%, TB-500 10%) allows researchers to examine additive or synergistic effects across multiple biochemical pathways relevant to cell signaling and structural integrity.

1. GHK-Cu: Gene Expression and Tissue Remodeling

GHK-Cu has been shown to modulate the expression of hundreds of genes related to:

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  • Tissue repair, collagen synthesis, and extracellular matrix remodeling
  • Anti-inflammatory signaling through inhibition of TNF-α and IL-6 expression [1]
  • Copper ion delivery into cells, promoting antioxidant enzyme function and cellular respiration [2]
Studies have used gene array profiling and RNA sequencing to document the changes GHK-Cu induces in fibroblasts, keratinocytes, and endothelial cells.

2. BPC-157: Angiogenesis and Cytokine Modulation

BPC-157 is widely used in models studying angiogenesis and vascular repair:

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  • Promotes vascular endothelial growth factor (VEGF) expression and endothelial cell proliferation [3]
  • Modulates cytokine levels, reducing IL-1β, IL-6, and TNF-α in inflamed tissue models
  • Demonstrated ability to support tendon fibroblast migration in rat explant studies [4]
Its stability in gastric juice and plasma allows for extended study windows in gastrointestinal and musculoskeletal research models.

3. TB-500: Cell Migration and Actin Regulation

TB-500 (the synthetic form of Thymosin Beta-4) is studied for its ability to:

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  • Regulate actin polymerization, enhancing cell motility and wound closure [5]
  • Promote angiogenesis through upregulation of VEGF and other pro-vascular signals
  • Reduce oxidative stress and tissue fibrosis in preclinical cardiac and dermal models [6]
Researchers frequently use TB-500 to model tissue regeneration, particularly in cardiovascular, muscular, and epithelial contexts.

Synergistic Applications of the GLOW Blend

The combination of these three peptides in GLOW supports advanced studies in:

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  • Wound healing and epithelial regeneration
  • Angiogenic and anti-inflammatory signaling
  • Fibroblast migration and collagen matrix production
  • Neurovascular remodeling and tissue oxygenation
Co-administration in this ratio enables researchers to evaluate multi-pathway peptide crosstalk and downstream transcriptional effects using in vitro and animal model systems.

Referenced Citations

  1. Pickart L, et al. “GHK-Cu stimulates wound healing and gene expression in skin fibroblasts.” Journal of Biomaterials Science, 2008. – PubMed
  2. Pickart L, et al. “Copper peptide GHK and tissue regeneration: gene expression profiling.” Molecular Genetics and Metabolism, 2012. – PubMed
  3. Sikiric P, et al. “BPC-157 and angiogenesis: novel peptide mechanisms.” Current Pharmaceutical Design, 2014. – PubMed
  4. Chang CH, et al. “BPC-157 enhances fibroblast migration and tendon healing in rats.” Journal of Orthopaedic Research, 2011. – PubMed
  5. Goldstein AL, et al. “Thymosin beta-4 promotes tissue regeneration by actin modulation.” Annals of the New York Academy of Sciences, 2007. – PubMed
  6. Smart N, et al. “Thymosin beta-4 and cardiac repair: angiogenesis and anti-fibrotic activity.” Nature, 2007. – PubMed

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