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A short-acting growth-hormone-releasing-hormone analog without the drug-affinity complex. Studied for pulsatile GH release in research models.
CJC-1295 (no DAC) is a synthetic 30-residue analog of GHRH(1-29) with four amino acid substitutions (D-Ala²/Gln⁸/Ala¹⁵/Leu²⁷) that enhance plasma stability and GHRH-receptor potency. Without the drug-affinity complex (DAC) modification, the peptide retains the natural pulsatile pharmacokinetics of GHRH agonism.
Each vial is lyophilized from acetate buffer, sealed under nitrogen, and shipped cold-chain at −20 °C from our Kelowna facility.
GHRH-receptor binding assays, in-vitro pituitary GH-secretion screens, and comparative pharmacokinetics versus DAC-modified analogs and natural GHRH(1-29).
Sold for laboratory research only. This material is not a drug, food, or cosmetic and is not intended for diagnostic, therapeutic, or recreational use.
| Parameter | Value |
|---|---|
| Sequence | Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-NH₂ |
| Molecular formula | C₁₅₂H₂₅₂N₄₄O₄₂ |
| Molecular weight | 3367.93 g/mol |
| CAS number | 863288-34-0 |
| Length | 30 residues |
| Test | Specification |
|---|---|
| HPLC purity | ≥ 99.0% (lot LM-2615: 99.21%) |
| Mass confirmation | ESI-MS within 0.5 Da |
| Net peptide content | ≥ 80% by AAA |
| Endotoxin | < 0.5 EU/mg (LAL) |
| Bioburden | < 10 CFU/g |
| Residual TFA | < 1.0% |
Manufactured 04 Mar 2026 · Released 11 Mar 2026 · Tested by Lumera QC, Kelowna BC. Retain samples held under storage spec for five years from release date.
| Method | Result |
|---|---|
| RP-HPLC at 220 nm | 99.21% main peak |
| ESI-MS (positive) | 3367.9 Da (theor. 3367.93) |
| Amino acid analysis | 82.1% net peptide |
| LAL endotoxin | < 0.05 EU/mg |
| Karl Fischer (water) | 2.8% w/w |
Allow vial to reach room temperature before opening (≥ 20 minutes). Reconstitute with 1.0–2.5 mL of sterile bacteriostatic water (0.9% benzyl alcohol). Inject solvent slowly down the inner wall of the vial; do not direct stream onto the lyophilized cake.
Swirl gently for 30 seconds. Do not vortex. Allow to dissolve for 5 minutes; clarity should be complete with no visible particulates.
Reconstituted solution is stable for 28 days at 2–8 °C in original vial. For longer storage, aliquot into low-binding tubes and hold at −80 °C; avoid repeated freeze-thaw cycles. Discard if turbidity, color change, or particulate matter is observed.
Teichman SL et al. Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295. J Clin Endocrinol Metab. 2006;91(3):799–805.
Sackmann-Sala L, Kopchick JJ. Growth hormone receptor signaling and disease. Mol Cell Endocrinol. 2014;392(1-2):1–8.
Veldhuis JD, Bowers CY. Integrating GHRH agonism and ghrelin-receptor agonism. Endocrine. 2010;38(1):1–16.
CJC-1295 No DAC reference standard, ≥99% (HPLC), Lumera Labs Inc., Cat. No. LUM-CJC1295-5, Lot 26-A031.
Cjc 1295 is a GHRH analog, classified within the growth-axis signaling pathway. Structurally it is a 30-residue D-Ala-modified GHRH. CJC-1295 (no DAC) is a synthetic 30-residue analog of growth-hormone-releasing hormone (GHRH 1-29) with substitutions at positions 2, 8, 15, and 27 conferring DPP-IV resistance and extended half-life. Teichman et al. (2006) characterized its pharmacokinetics.
In an in-vitro setting, Cjc 1295 interacts with its target receptor(s) at low-nanomolar affinities under standard binding-assay conditions. Reconstitution should be performed in sterile bacteriostatic water at the working concentration your protocol specifies; the lyophilized vial is sealed under nitrogen and stable at −20 °C until reconstituted.
Cjc 1295 arrives lyophilized at −20 °C in cold-chain insulated packaging. On receipt, transfer immediately to a −20 °C freezer. Once reconstituted, store at 2-8 °C and use within the window noted on the lot's COA. Avoid repeated freeze-thaw cycles.
For laboratory research only. Cjc 1295 is sold strictly as an in-vitro reference standard. It is not approved for human or veterinary use by Health Canada or the FDA.