Radiance Research
GHK-CU 100mg
100mg
GHK-Cu is a naturally occurring tripeptide-copper complex — glycyl-L-histidyl-L-lysine chelated to a copper(II) ion — first isolated from…
$80.00
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Lot 20260303glo
99.573% · Freedom Diagnostics · 2026-03-07Report 2603060167 · 10/10/50mg
For research use only — not for human or animal use.
Radiance
GLOW
$130.00
Strength · 70mg
GLOW Blend 70mg lyophilized vial — 50mg GHK-Cu + 10mg BPC-157 + 10mg TB-500. For in-vitro research into ECM remodeling and angiogenesis.
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Research Notice
For laboratory research use only. Not for human consumption.
The Dossier
Research Notes
GLOW is a co-lyophilized research blend that assembles three complementary tissue-remodeling references into a single vial: GHK-Cu (copper tripeptide-1), BPC-157, and TB-500. Its copper-tripeptide-dominant composition gives the powder a characteristic pale-blue tint.
It is studied for the combined signaling characteristics of its constituents in comparative models, consolidating three gold-standard references into one acquisition for laboratory convenience.
Research Focus
- Dermal wound-healing and re-epithelialization models
- Tendon, ligament, and skeletal-muscle repair models
- Angiogenesis (ischemia) models
- Dermatology and hair-follicle research
- Anti-inflammatory and antioxidant models
Mechanism
The three components engage distinct, non-overlapping repair axes: GHK-Cu as a copper-delivery vehicle and broad gene modulator of extracellular-matrix synthesis; BPC-157 through VEGFR2-associated angiogenic signaling; and TB-500 through actin sequestration and cytoskeletal remodeling.
Convergent axes characterized across the single-agent literature include Nrf2/Keap1 antioxidant signaling and NF-κB modulation.
Storage & Handling
Store the lyophilized blend at −20°C for long-term stability. Reconstituted solution is held cold and used within a short window; avoid chelating agents, which can strip copper from the GHK-Cu component.
References
- Pickart L, Margolina A. Regenerative and protective actions of the GHK-Cu peptide in light of new gene data. Int J Mol Sci. 2018.
- Hsieh MJ, et al. Therapeutic potential of pro-angiogenic BPC157 is associated with VEGFR2 activation. J Mol Med. 2017.
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