
2X Blend CJC-1295 Without DAC / Ipamorelin
The 2X Blend combines CJC-1295 Without DAC and Ipamorelin — the standard GHRH+GHRP research combination producing synergistic, selective GH pulse amplification through two independent receptor systems.
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MOD GRF 1-29 (CJC-1295 Without DAC) is a tetrasubstituted GHRH(1-29) analog with ~30-minute half-life — the most commonly used short-acting GHRH compound for pulsatile GH secretion research.
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Lyophilized vial
Sterile-filtered, freeze-dried peptide in glass vial, sealed under inert gas.
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Third-party HPLC tested
Every lot is tested for identity and purity by an independent analytical lab. Certificate of Analysis available on request, tied to the exact lot you receive.
Lyophilized and lot-tracked
Sterile-filtered, freeze-dried, sealed under inert gas. Each vial carries its own lot ID — full chain of custody from fill to delivery.
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How it works
MOD GRF 1-29 activates GHRH receptors on pituitary somatotropes with full agonism, producing pulsatile GH release via cAMP signaling. Four protective substitutions extend half-life from ~2 min to ~30 min by blocking DPP-IV and neutral endopeptidase cleavage. Synergistic with GHS-R1a agonists (ipamorelin) through mechanistically independent GH amplification.
Compound profile
Product definition
MOD GRF 1-29 (CJC-1295 Without DAC) is a tetrasubstituted GHRH(1-29) analog with ~30-minute half-life — the most commonly used short-acting GHRH compound for pulsatile GH secretion research.
MOD GRF 1-29 is the pharmacological name for the tetrasubstituted GHRH(1-29) peptide. The 'MOD' prefix indicates the four protective modifications: Aib at position 2 (DPP-IV resistance), Gln at position 8 (neutral endopeptidase protection), Ala at position 15 (backbone stability), and Nle at position 27 (methionine oxidation prevention). These modifications are collectively responsible for the pharmacokinetic improvement versus native GHRH while preserving receptor binding and signaling. The compound is also commercially designated CJC-1295 Without DAC — the same peptide referenced by the ConjuChem nomenclature used in research supply contexts. For researchers cross-referencing the pharmacological literature versus commercial product catalogs, MOD GRF 1-29 and CJC-1295 Without DAC are fully interchangeable terms for the same molecule. In the GH secretagogue research literature, MOD GRF 1-29 is studied both as a standalone GHRH agonist (characterizing GHRH receptor pharmacology) and in combination with GHRPs (characterizing the synergistic GHRH+GHRP GH amplification effect). Its 30-minute half-life and preserved pulsatile kinetics make it the default short-acting GHRH reference compound.
Research audience
MOD GRF 1-29 is used by researchers in GH axis pharmacology, GHRH receptor biology, pituitary somatotrope function, and GH secretagogue combination research. It is the standard GHRH component for researchers who are cross-referencing pharmacological literature (where 'MOD GRF 1-29' is the primary designation) with commercial research supply sources.
Research context
The pharmacological development of MOD GRF 1-29 represents the systematic application of protective amino acid substitution technology to native GHRH(1-29) — the same approach used in semaglutide (position-8 Aib substitution for DPP-IV resistance) applied to the GHRH scaffold. The specific substitutions were chosen based on known enzymatic cleavage sites in native GHRH: DPP-IV cleavage at His-Ala at positions 1-2, neutral endopeptidase action at position 8, and oxidative methionine degradation at position 27. In GH pulse biology research, MOD GRF 1-29 is used to study how GHRH receptor activation patterns affect somatotrope GH secretion. The pulsatile kinetics (on for ~30 min, then cleared) allow researchers to characterize the GH response to a defined, time-limited GHRH receptor stimulus — useful for studies of somatotrope desensitization, GHRH receptor downregulation, and the pulse frequency effects on downstream IGF-1. For combination GHRH+GHRP research (the 2X Blend design), MOD GRF 1-29 is the GHRH component that pairs with ipamorelin. The mechanistic model is: GHRH receptor activation recruits additional somatotropes and increases their responsiveness (the 'priming' effect); GHS-R1a activation by ipamorelin then produces a larger GH release from the primed pool. The result is a synergistic GH pulse that exceeds either compound alone.
Common questions
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2X Blend CJC-1295 Without DAC / Ipamorelin
The 2X Blend combines CJC-1295 Without DAC and Ipamorelin — the standard GHRH+GHRP research combination producing synergistic, selective GH pulse amplification through two independent receptor systems.

CJC-1295 Without DAC
CJC-1295 Without DAC (MOD GRF 1-29) is a tetrasubstituted GHRH(1-29) analog with ~30-minute half-life — the preferred short-acting GHRH analog for pulsatile GH research protocols, commonly paired with ipamorelin.

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Research Use Only
Sold for laboratory and research purposes only. Not approved for, nor intended for, human or veterinary consumption, diagnostic use, or therapeutic application. These products have not been evaluated by the Food and Drug Administration. Keep out of reach of children. For use by qualified researchers only.
Nothing on this page constitutes medical advice, a treatment recommendation, or a clinical protocol. Consult a qualified healthcare provider before making any health or treatment decisions.
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