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GLOW

GLOW

Base Peptides are intended for licensed medical professionals and experienced researchers. Reconstitution required. Dosing and use instructions are not provided.

Regular price $90.00
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GLOW — GHK-Cu + BPC-157 + TB-500 Research Blend

GLOW combines three complementary research peptides—GHK-Cu (copper-binding tripeptide), BPC-157 (gastric “Body Protection Compound” fragment), and TB-500 (Thymosin-β4 research fragment). The blend is designed for laboratories exploring ECM/tissue remodeling, barrier integrity, cell migration, and angiogenic signaling in skin, tendon/ligament, and endothelial models.

Component A — GHK-Cu
  • Core motif: Gly-His-Lys·Cu(II) (tripeptide–copper complex)
  • Focus: ECM gene programs (collagens, integrins), antioxidant/metal-binding context, fibroblast & keratinocyte endpoints.
  • Notes: Copper coordination is central—document buffer and pH in your methods.
Component B — BPC-157
  • Sequence (15 aa): GEPPPGKPADDAGLV
  • Focus: Epithelial/endothelial barrier metrics, cytokine balance, migration and tubulogenesis assays.
  • Notes: Often examined in TEER, tight-junction, and wound-closure models.
Component C — TB-500 (Thymosin-β4 fragment)
  • Parent protein: Thymosin-β4 (43 aa)
  • Focus: Actin binding & cytoskeletal dynamics, cell motility, angiogenic sprouting.
  • Notes: Useful for dissecting migration speed, focal-adhesion turnover, and sprout length.

Why This Blend (Plain English)

Complementary Mechanisms

  • GHK-Cu → ECM & trophic gene expression; matrix organization.
  • BPC-157 → Barrier support & angiogenic cues.
  • TB-500 → Motility and actin-cytoskeleton remodeling.

Design Advantages

  • Run a single protocol to capture matrix + barrier + migration endpoints.
  • Adjust ratios to emphasize ECM (GHK-Cu), barrier (BPC-157), or motility (TB-500).
  • Add single-agent control arms to quantify additivity vs synergy.

Potential Research Applications

Dermal/ECM Panels

  • Collagen I/III, elastin, laminin; MMP/TIMP balance
  • Fibroblast proliferation & morphology

Barrier & Endothelium

  • TEER (tight-junction integrity), permeability assays
  • VE-cadherin, ZO-1, occludin readouts

Migration & Angiogenesis

  • Scratch/wound-closure, live-cell motility tracking
  • Tubulogenesis & 3D sprouting assays

Blend Options (Research Configurations)

Standard

  • 1:1:1 (GHK-Cu : BPC-157 : TB-500)
  • Balanced ECM, barrier, and motility coverage

Dermal/ECM-Forward

  • 2:1:1 (GHK-Cu heavy)
  • Emphasis on collagen & matrix transcripts

Barrier-Forward

  • 1:2:1 (BPC-157 heavy)
  • Emphasis on TEER and epithelial endpoints

Motility-Forward

  • 1:1:2 (TB-500 heavy)
  • Emphasis on actin dynamics & migration speed

Design Notes

  • State salt/form for each component (e.g., GHK-Cu complex, BPC-157 acetate, TB-500 acetate).
  • Document vehicle, pH, ionic strength, and serum lot—endpoints are condition-sensitive.
  • Include single-agent and vehicle controls for mechanism clarity.

Key Study Themes (Educational Summary)

GHK-Cu — matrix & trophic signaling
  • Frequently associated with up-regulating ECM and repair genes in skin/dermal models.
  • Consider copper-free controls to isolate metal-coordination effects.
BPC-157 — barrier biology & angiogenic cues
  • Reported effects on tight junction proteins and endothelial tubulogenesis.
  • Use TEER/permeability plus cytokine panels for a complete picture.
TB-500 — cytoskeleton & motility
  • Examined for effects on actin binding, migration speed, and sprouting length.
  • Pair imaging (phalloidin, vinculin) with functional migration endpoints.

Synergistic Peptides (for Study Design)

LL-37

  • Why pair: Epithelial defense & wound context to complement barrier/ECM work.
  • Angle: Co-culture wound models with cytokine readouts.

Tα1 (Thymosin-α1)

  • Why pair: Immune-modulation alongside repair endpoints.
  • Angle: Th1/Th2 panels + barrier metrics under challenge.

SS-31 (Elamipretide)

  • Why pair: Mitochondrial membrane support during repair stress.
  • Angle: Δψm/ATP metrics + migration/ECM assays.

Controls

  • Run GHK-Cu-only, BPC-only, TB-only arms to map contribution of each component.
  • Include copper chelator or metal-free conditions where relevant.

Known Concerns (Context)

  • Co-formulation: Verify compatibility (pH, buffer salts, chelators) so GHK can bind copper as intended and other peptides remain stable.
  • Stability: Prepare fresh aliquots; minimize freeze–thaw; protect from light/moisture.
  • Model variability: Outcomes can vary with substrate coatings, serum lots, and cell passage—document conditions tightly.
  • General: For laboratory research use only; not for human consumption or therapeutic use.

Specifications & Handling

  • Form: Lyophilized powders premixed (lot-coded); label indicates blend ratio
  • Purity (each): ≥ 99% (HPLC/MS verified)
  • Storage: ≤ −20 °C; dry, low-light conditions
  • In solution: Use sterile diluent; record pH/vehicle and time-to-use; aliquot immediately
  • Packaging: Tamper-evident; research-only labeling; copper content documented per lot

Regulatory & Use Notice

Sold for laboratory research use only. Not for human consumption, medical, or veterinary use. No human-use instructions are provided. Buyer is responsible for safe handling and regulatory compliance.

GLOW Research Blend | GHK-Cu + BPC-157 + TB-500 | ECM Remodeling, Barrier Integrity, Migration & Angiogenesis

Keywords: GHK-Cu peptide, BPC-157, TB-500, Thymosin beta-4 fragment, skin research peptide, ECM remodeling, wound-healing assays, angiogenesis, Base Peptides GLOW blend.

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Instructions are NOT provided before or after purchase.

Peptide molecules are unfinished and require reconstitution from a skilled and licensed professional to activate the compound into liquid form. Instructions are not provided for reconstitution, dosing, or adminstration. All products are strictly intended for research purposes and laboratory experimentation. Handling should be by skilled licensed and credentialed professionals only. Non experimental use is strictly prohibited.