Not for human use, for research purposes only
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CJC-1295 (no DAC) - CJC-1295 without DAC (Mod GRF 1-29) is a short-acting GHRH a

CJC-1295 (no DAC)

CJC-1295 without DAC (Mod GRF 1-29) is a short-acting GHRH analogue that binds the pituitary GHRH receptor (Gs/cAMP) on somatotrophs.

GH Axis
In Stock

1 vial · 10 mg total

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Total Price

฿1900

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For research & laboratory use only. Not for human consumption.

Shipping: free within Thailand, ฿700 worldwide. Added at checkout. Delivery times & countries

Half-Life

~30 minutes

Short-Acting GHRH Analogue

Binds the pituitary GHRH receptor, a Gs-coupled receptor

Modified GRF 1-29 Structure

Four amino-acid substitutions at positions 2, 8, 15 and 27

Thirty-Minute Half-Life

Without the Drug Affinity Complex, clearance stays rapid

Mechanism of Action

CJC-1295 without DAC, also known as Modified GRF 1-29, is a stabilised fragment of growth-hormone-releasing hormone (GHRH 1-29) carrying four amino-acid substitutions that block enzymatic breakdown without the albumin-binding Drug Affinity Complex. It binds the pituitary GHRH receptor on somatotroph cells and couples through the Gs protein to activate adenylyl cyclase, raising intracellular cAMP and amplifying growth-hormone synthesis and release. Because no DAC is attached, the peptide clears in roughly 30 minutes, in contrast to the DAC-bound version with its multi-day half-life.

Research Overview

CJC-1295 without DAC, the Modified GRF 1-29 peptide, is a short-acting GHRH analogue and a frequent reference compound wherever physiological GHRH receptor signalling matters. Common research areas:

  • Pulsatile growth-hormone release and somatotroph signalling studies
  • GHRH receptor sensitivity and tachyphylaxis comparisons against DAC-bound analogues
  • Receptor comparisons with GHRP-class secretagogues such as ipamorelin
  • Structure and stability work on modified GHRH fragments

The Four Amino-Acid Substitutions

Mod GRF 1-29 differs from native GHRH(1-29), the same active fragment marketed as Sermorelin, at four positions. Each change closes a specific degradation pathway:

  1. Position 2: Ala to D-Ala, which resists DPP-4 cleavage at the N-terminus
  2. Position 8: Asn to Gln, which prevents asparagine deamidation
  3. Position 15: Gly to Ala, which reduces flexibility at a vulnerable site
  4. Position 27: Met to Leu, which prevents methionine oxidation

Together these substitutions extend the half-life from roughly 7 minutes for Sermorelin to about 30 minutes for CJC-1295 no DAC, with equivalent or better receptor potency.

Receptor Comparison with Ipamorelin

CJC-1295 no DAC and ipamorelin act on different receptors of the same pituitary somatotroph:

  • The GHRH receptor (Gs-coupled), the target of CJC-1295 no DAC, raises cAMP
  • The ghrelin receptor GHS-R1a (Gq-coupled), the target of ipamorelin, raises intracellular Ca2+

Milo-Lab lists an Ipamorelin + CJC-1295 blend as a separate product.

Storage

Lyophilised vials: store at -20°C, protected from light.

For research purposes only. Not for human consumption.

Product FAQs

Listed in Blends

GH Axis Blend

Ipamorelin CJC-1295 (no DAC)
View Blend Research

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