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GHK-cu | 100mg

GHK-cu | 100mg

Regular price $59.00
Regular price $59.00 Sale price
SAVE Sold out

check_circle Enhanced Tissue Remodeling

check_circle Guaranteed >99% Purity

check_circle High-Potency 100mg

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Research Disclaimer: Not for human or Veterinary Consumption

GHK-cu | 100mg

GHK-cu | 100mg

Regular price $59.00
Regular price $59.00 Sale price
SAVE Sold out

Description

Regeneration. Structure. Purity.

VitraNova Research introduces GHK-cu Core, a high-concentration 100mg formulation of the copper-binding peptide GHK (glycyl-L-histidyl-L-lysine). Widely researched for its role in tissue remodeling and collagen synthesis, our GHK-cu is synthesized to meet the rigorous demands of laboratory investigation.

Each vial contains a substantial 100mg quantity of the compound, verified to meet or exceed 99% purity for consistent experimental results.

  1. High Potency: 100mg of active research reagent per vial.
  2. Purity Verified: >99% purity confirmed via analysis.
  3. Research Grade: Formulated strictly for laboratory use.
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Specifications

Product Name: GHK-Cu Core

Net Content: 100 mg

Compound Type: Copper-binding tripeptide (Glycyl-L-Histidyl-L-Lysine)

Purity: >99% (analytically verified)

Form: Lyophilized powder

Grade: Research use only

Potency: High-potency 100 mg active compound

Packaging: Medical-grade glass vial

Stability: Lyophilized to preserve chelation integrity

Intended Use: Tissue remodeling, collagen synthesis, and extracellular matrix research

Storage: Store in a cool, dry place away from light

Compliance: Not for human or veterinary consumption

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Optimizing Collagen and Extracellular Matrix Research

VitraNova Research presents GHK-cu Core as a definitive reagent for studying tissue regeneration and structural integrity. As a copper-binding tripeptide (glycyl-L-histidyl-L-lysine), GHK-cu is critical for investigating the upregulation of collagen, elastin, and glycosaminoglycans. Our formulation preserves the peptide’s chelation properties, enabling researchers to precisely evaluate its influence on wound healing cascades, antioxidant enzyme activation, and the remodeling of the extracellular matrix without the variability introduced by unstable compounds