GP10(CJC-1295 Without DAC 5mg + Ipamorelin 5mg)

CJC-1295 (No DAC) 5mg + Ipamorelin 5mg blend is a research-grade, lyophilized peptide combination designed to synergistically stimulate growth hormone (GH) secretion via dual activation of the GHRH receptor and GHS-R1a (ghrelin receptor). Formulated for preclinical studies in anti-aging, muscle regeneration, metabolic modulation, and tissue recovery, this 1:1 ratio delivers a physiologically patterned GH pulse—mimicking the body’s natural GH release pattern to elevate IGF-1 levels.

10mg*10vials $95

Product Information

What is GP10? (Full Composition & Profile)

 

CJC-1295 Without DAC (5mg)

  • Full Name: Modified GRF (1–29), CJC-1295 No DAC (Drug Affinity Complex)
  • Class: GHRH (growth hormone-releasing hormone) analog
  • Structure: 29-amino-acid peptide with 4 stabilizing modifications; no long-chain DAC extension
  • Half-life: ~30 minutes – 2 hours (short-acting, pulse-restricted)
  • Purity: ≥99% (HPLC validated)

Ipamorelin (IPA, 5mg)

  • Class: Selective GHS (growth hormone secretagogue), pentapeptide
  • Sequence: Aib-His-D-2-Nal-D-Phe-Lys-NH₂
  • Half-life: ~1–2 hours
  • Key Selectivity: Does not elevate cortisol, prolactin, or ACTH (unlike GHRP-2/GHRP-6)

GP10 Blend Specifications

  • Total: 10mg lyophilized powder (5mg + 5mg 1:1 ratio)
  • Form: Sterile lyophilized cake; reconstitute with bacteriostatic water (BAC) or 0.9% saline
  • Storage:
    • Unreconstituted: −20°C, dry, dark (stable ≥2 years)
    • Reconstituted: 2–8°C, use within 30 days; avoid freeze–thaw

Target Research Populations & Applications

 
GP10 is optimized for preclinical models studying:
 
  • Age-related GH/IGF-1 decline (sarcopenia, frailty, impaired recovery)
  • Muscle & soft-tissue repair: tendon/ligament injury, post-surgical recovery, muscle wasting
  • Metabolic research: body composition (fat loss + lean mass retention), insulin sensitivity
  • Anti-aging & regenerative biology: skin aging, wound healing, neuroprotection
  • Endocrine pharmacology: GH pulse dynamics, pituitary receptor crosstalk

 

Mechanism of Action (Dual-Path Synergy)

 

CJC-1295 No DAC (GHRH Pathway)

  • Binds pituitary GHRH receptors → activates cAMP/PKA → GH vesicle exocytosis
  • Increases amplitude of natural GH pulses (sharp, physiological peaks)
  • Avoids receptor desensitization (short half-life preserves pulsatility)

Ipamorelin (GHS-R1a Pathway)

  • Activates pituitary ghrelin (GHS-R1a) receptors → Ca²⁺ influx → GH secretion
  • Inhibits somatostatin (the endogenous GH “brake”) → increases frequency of GH pulses
  • Ultra-selective: no HPA-axis activation or prolactin rise

GP10 Synergistic Effect (1+1 > 2)

  • Amplitude (CJC) + Frequency (IPA)sustained, physiological GH/IGF-1 elevation (2–5× baseline)
  • No hormonal interference: clean GH/IGF-1 signal without cortisol/prolactin side effects
  • Downstream effects: angiogenesis, collagen synthesis, cell proliferation, anti-inflammation, anti-apoptosis

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