CJC-1295 ipamorelin is a co-formulated research blend of two synthetic peptides that act on two different pituitary receptors: CJC-1295 without DAC (Modified GRF(1-29), CAS 863288-34-0, C152H252N44O42, 3367.95 g/mol) is a 29-residue analog of growth-hormone-releasing hormone that binds the GHRH receptor, and ipamorelin (CAS 170851-70-4, C38H49N9O5, 711.9 g/mol) is a five-residue ghrelin mimetic that binds the growth-hormone secretagogue receptor GHS-R1a; the blend is supplied as a 5 mg / 5 mg lyophilized powder for in vitro receptor and cell-signaling research. This profile covers what each component is, why the two are co-formulated, how the pair is studied in receptor-expressing cells, and how a laboratory confirms both components are present at the stated ratio.
What is in the CJC-1295 / ipamorelin blend?
The Ipamorelin/CJC-1295 (no DAC) vial contains two chemically unrelated peptides that happen to converge on the same cell type. One is long and helical; the other is short and heavily modified. The catalog lists them at 5 mg each, and the lot-specific ratio is printed on the Certificate of Analysis.
| Component | Class | Length | Receptor | CAS | Formula | MW (g/mol) |
|---|---|---|---|---|---|---|
| CJC-1295 no DAC (Modified GRF(1-29)) | GHRH analog | 29 residues | GHRH-R (class B GPCR) | 863288-34-0 | C152H252N44O42 | 3367.95 |
| Ipamorelin | Ghrelin mimetic (GHRP) | 5 residues | GHS-R1a (class A GPCR) | 170851-70-4 | C38H49N9O5 | 711.9 |
Because the two molecular weights differ by almost five-fold, equal masses are not equal molar amounts: 5 mg of ipamorelin is about 7.0 micromoles, while 5 mg of CJC-1295 no DAC is about 1.5 micromoles. Any experiment that compares the two must be planned in molarity, not milligrams.
What is CJC-1295 no DAC?
CJC-1295 no DAC is the 29-residue amino-terminal fragment of GHRH with four residues substituted: D-alanine at position 2, glutamine at 8, alanine at 15 and leucine at 27, and a C-terminal carboxamide. Full 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. The substitutions remove the dipeptidyl-peptidase-IV cleavage site at Ala2-Asp3 and replace oxidation- and deamidation-prone residues, which is why the analog is far more stable in assay buffer than native GHRH(1-29). The chemistry is covered in detail in CJC-1295 explained: Modified GRF(1-29) and the DAC modification. The catalog form carries no Drug Affinity Complex; the difference is laid out in CJC-1295 with DAC vs no DAC.
What is ipamorelin?
Ipamorelin is a synthetic pentapeptide, Aib-His-D-2-Nal-D-Phe-Lys-NH2, in which three of five residues are non-proteinogenic. It is a growth-hormone secretagogue receptor agonist, a ghrelin mimetic, and is noted in the literature for its selectivity for GHS-R1a over other receptor systems. Its structure and handling are profiled in ipamorelin peptide: pentapeptide structure and stability, and its receptor selectivity in ipamorelin and GHS-receptor selectivity.
Why are a GHRH analog and a ghrelin mimetic co-formulated?
The two receptors sit on the same somatotroph cell but signal through different G proteins. GHRH-R couples to Gs and raises cyclic AMP; GHS-R1a couples mainly to Gq/11 and raises intracellular calcium through phospholipase C. In pituitary cell models the two inputs are not simply additive, and the question of how a cAMP signal and a calcium signal combine in one cell is the central reason the pair is studied together. The experimental logic is developed in why pair a GHRH analog with a GHRP? and the broader receptor-class comparison in GHRH analogs vs GH secretagogues.
How is the blend used in vitro?
Typical designs run each component alone and the two together at matched molar concentrations in cells expressing one or both receptors: HEK293 or CHO cells transfected with GHRH-R or GHS-R1a for single-receptor pharmacology, and primary or immortalized pituitary cells for the combined readout. Measurements are cAMP accumulation (HTRF or ELISA), calcium flux (Fluo-4 or aequorin) and CRE- or SRE-driven reporter expression, always against vehicle and single-agonist controls. Methods are described in GPCR binding assays in vitro.
How do you confirm both peptides are in the vial?
A two-component blend needs a COA that reports each peptide separately. HPLC should show two principal peaks with individual purity values, and mass spectrometry should show ipamorelin at [M+H]+ about 712.9 and CJC-1295 no DAC as a multiply charged envelope ([M+3H]3+ about 1123.6, [M+4H]4+ about 843.0). The sourcing checklist and the 5 mg / 5 mg reconstitution math are in sourcing a two-component blend: COA and ratio verification.
Related research guides
- CJC-1295 explained: Modified GRF(1-29) and the DAC modification
- CJC-1295 with DAC vs no DAC: structure and stability differences
- Why pair a GHRH analog with a GHRP? Dual-receptor pituitary cell assays
- Sourcing a two-component blend: COA and ratio verification (5/5 mg)
- Ipamorelin peptide: pentapeptide structure and stability
- GHS-receptor signaling in vitro: the ghrelin receptor pathway
Research-use note
All materials discussed are supplied for in vitro laboratory research use only, and are not for human or animal use.








