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CJC-1295 No DAC (Modified GRF 1-29)

High Purity Peptide — 5mg & 10mg

$60.00

CJC-1295 No DAC (Modified GRF 1-29)

Available in 5mg & 10mg Lyophilized Vials

Short-Acting GHRH Secretagogue | The "Pulsatile" Agent

The 4Balance Codex: The Architect of Physiological, Pulsatile Growth Hormone Dynamics.

Product Overview

CJC-1295 No DAC, frequently cited in literature as Modified GRF 1-29, is a synthetic, tetrasubstituted 29-amino acid analogue of endogenous Growth Hormone-Releasing Hormone (GHRH).

This peptide is distinguished by the absence of the "Drug Affinity Complex" (DAC) linker found in its long-acting counterpart. Without the DAC tail to bind serum albumin, this analogue possesses a significantly shorter half-life (~30 minutes in research models).

CJC-1295 No DAC is the premier research tool for investigators seeking to replicate physiological, pulsatile Growth Hormone (GH) secretion patterns, avoiding the chronic, continuous elevation associated with long-acting agents. We offer this essential research compound in both 5mg and 10mg formats to suit various experimental scales.

Mechanism of Action: Engineered Stability & Natural Rhythm

CJC-1295 No DAC is designed to overcome the rapid degradation of native GHRH while maintaining a natural secretory profile.

  • Enhanced Enzymatic Stability (The "Modified" Aspect): Native GHRH (1-29) is rapidly degraded by the enzyme dipeptidyl peptidase-IV (DPP-IV). CJC-1295 No DAC incorporates four strategic amino acid substitutions (D-Ala2, Gln8, Ala15, Leu27). These modifications render it highly resistant to DPP-IV cleavage, significantly increasing its in vivo bioactivity compared to unmodified Sermorelin.

  • Mimicry of Endogenous Rhythms (The "No DAC" Aspect): By lacking the albumin-binding DAC tail, this peptide prevents a long-term "GH bleed." Instead, it allows researchers to stimulate distinct peaks of GH followed by necessary troughs. This mimics the body's natural circadian and ultradian rhythms, a crucial factor for maintaining pituitary receptor sensitivity and avoiding tachyphylaxis (desensitization).

  • Selective GHRH Receptor Agonism: The peptide binds specifically to the GHRH receptor (GHRH-R) in the anterior pituitary gland, triggering cAMP signaling to release stored growth hormone in a distinct pulse.

Primary Research Applications

In the 4Balance Research Array, CJC-1295 No DAC is the preferred agent for studies requiring precise temporal control over GH release.

  • Physiological GH Dynamics: Used to model natural, spike-dependent GH signaling and its downstream effects on IGF-1 levels, lipolysis, and protein synthesis without causing pituitary desensitization.

  • Synergistic Secretagogue Studies: Frequently utilized in combination protocols with Ghrelin mimetics (GHRPs such as Ipamorelin or GHRP-6) to investigate the synergistic amplification of pituitary GH output via simultaneous activation of distinct enzymatic pathways.

  • Sleep Architecture & Circadian Rhythm: Because endogenous GH secretion peaks during slow-wave sleep, the short half-life of this compound makes it ideal for sleep-related endocrine research protocols.

Technical Specifications

  • Format: Lyophilized Powder

  • Options: Available in 5mg or 10mg vials

  • Sequence Length: 29 Amino Acids (Tetrasubstituted modification)

  • Molecular Formula: C₁₅₂H₂₄₃N₄₇O₄₂

  • Molecular Weight: 3367.9 g/mol

  • Solubility: Water Soluble (Requires Bacteriostatic Water for reconstitution)

  • Storage: Store lyophilized at -20°C. Reconstituted peptide should be kept at 4°C and used within established research timelines to maintain peak bioactivity.

Key References

  1. Campbell, R. M., et al. (1996). ORG 2766 and GRF analogs: peptide mediators of nerve regeneration and GH release. Peptides.

  2. Jetté, L., et al. (2005). Human Growth Hormone-Releasing Factor (hGRF)1–29-Albumin Bioconjugates Activate the GRF Receptor on the Anterior Pituitary in Rats: Identification of CJC-1295 as a Long-Lasting hGRF Analog. Endocrinology.

  3. Note on comparative literature: Teichman, S. L., et al. (2006) in The Journal of Clinical Endocrinology & Metabolism describes the DAC version, establishing the baseline for understanding why the "No DAC" version behaves differently regarding half-life.


DISCLAIMER: FOR RESEARCH USE ONLY. This product is a laboratory reagent intended strictly for in-vitro research and development. It is not for human consumption, veterinary use, or therapeutic application. Bodily introduction of any kind is strictly prohibited by law.

We pride ourselves on providing high quality products that are safe and effective. All of our research products are made with the highest quality ingredients, and undergo rigorous testing to ensure purity and potency.

CONTACT INFO

(864) 387-5929

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286 Rocky Creek Road
Greenville, SC 29615