CJC-1295 leads growth hormone secretion research through its DAC-modified GHRH(1-29) sequence, DPP-IV resistance, and extended half-life via albumin binding. The synthetic analog dominates pulsatile GH release, somatotroph signaling, and IGF-1 upregulation studies.
TOP RECOMMENDATION
CJC-1295 — GHRH(1-29) with Drug Affinity Complex
CJC-1295 is the leading peptide for growth hormone secretion research. As a DAC-modified GHRH(1-29) analog with D-Ala² DPP-IV resistance, it delivers sustained GH release kinetics through reversible albumin binding, with a half-life of 6–8 days versus minutes for native GHRH. Published studies demonstrate CJC-1295 stimulates cAMP-mediated GH secretion from anterior pituitary somatotrophs, upregulates IGF-1 in hepatocyte cultures, and maintains elevated GH pulsatility over multi-day observation windows. Tesamorelin, a full-length GHRH(1-44) analog with trans-3-hexenoic acid conjugation, offers the complete native receptor-binding domain for physiologically comparative studies but is more expensive, more complex to synthesize, and provides shorter-duration signaling. For GH secretion kinetics, IGF-1 upregulation, and metabolic pathway research, CJC-1295’s extended half-life, lower cost, and higher purity make it the definitive choice.
| RESEARCH APPLICATION | CJC-1295 | Tesamorelin |
|---|---|---|
| GH Secretion from Somatotrophs | ||
| IGF-1 Upregulation | ||
| Pulsatile Release Kinetics | ||
| DPP-IV Resistance | ||
| Albumin Binding (Extended t½) | ||
| Metabolic Stability | ||
| Cost per Experiment | ||
| Physiological Relevance (Full GHRH) |
RUNNER-UP
Tesamorelin — GHRH(1-44) Analog — Trans-3-Hexenoic Acid Conjugate
Consider when:
Compound
GHRH(1-29) with Drug Affinity Complex
CAS Number
863288-34-0
Purity (HPLC)
≥ 99.6%
Molecular Weight
3,367.97 g/mol
Sequence
Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser
Verification
HPLC + MS per batch
CJC-1295 is a DAC-modified GHRH(1-29) analog with DPP-IV resistance and albumin-binding extended half-life (6–8 days). It delivers sustained GH release at lower cost and higher synthesis purity than Tesamorelin. Tesamorelin is a full-length GHRH(1-44) analog with different stability kinetics — superior for physiological comparative studies, but less practical for sustained-release kinetics research.
For GH3 rat pituitary somatotrophs or primary anterior pituitary cell cultures, CJC-1295 is typically evaluated at 0.1–10 mcg/ml in serum-free DMEM/F12. GH secretion is measured by radioimmunoassay or ELISA at 1, 3, 6, and 24 hours. Include a GHRH antagonist control (e.g., astemizole) and vehicle control for mechanistic validation.
Yes. CJC-1295 stimulates GH secretion from somatotrophs, which in turn upregulates IGF-1 expression in hepatocytes (HepG2, primary human hepatocytes) via the JAK2/STAT5 pathway. Typical IGF-1 readouts (ELISA, qPCR) show significant upregulation at 24–72 hours in co-culture or conditioned media transfer models.
The Drug Affinity Complex (DAC) is a reactive group conjugated to the C-terminus of GHRH(1-29) that forms a reversible covalent bond with serum albumin. This albumin binding protects the peptide from renal clearance and proteolytic degradation, extending the half-life from minutes (native GHRH) to 6–8 days.
Yes. Many researchers use both as comparative GHRH analog controls. CJC-1295 represents the truncated, stabilized analog approach; Tesamorelin represents the full-length, conjugated analog approach. Reconstitute each separately and normalize by molar concentration (not mass) due to their different molecular weights.
TOP RECOMMENDATION
CJC-1295
GHRH(1-29) with Drug Affinity Complex
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RESEARCH USE ONLY. All compounds are strictly for in-vitro laboratory research by qualified professionals. Not for human consumption, veterinary use, or clinical application.