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CJC-1295 (with DAC)

CJC-1295 (with DAC)

Research Peptide | Lyophilized Powder | Batch Tested

Tested for
Purity
Size
$75.00
$3.75/mg
In StockLatest batch: CD2-260601
1

For laboratory research use only. Not for human or animal consumption. Insulated shipping · Styrofoam box available.

Product Overview

CJC-1295 (with DAC) is a GHRH analog carrying a Drug Affinity Complex — a chemical group that binds covalently to serum albumin — which extends its half-life from minutes to several days. This makes it a model compound for studying continuous, long-duration GHRH stimulation.

Batch CD2-260601Tested Jun 1, 2026
TestResultStatus
Purity98.5%Passed ✓
Batch CD5-260601Tested Jun 1, 2026
TestResultStatus
Purity98.5%Passed ✓
Batch CD10-260601Tested Jun 1, 2026
TestResultStatus
Purity99.6%Passed ✓
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Research Information

The DAC version is used to study sustained GHRH-receptor stimulation and the resulting elevation of baseline GH and IGF-1 levels over days in preclinical models. It lets researchers contrast continuous "GH bleed" against the pulsatile release produced by short-acting secretagogues. Supplied strictly for in-vitro and laboratory research use only — not for human or animal consumption.

CJC-1295 (with DAC) Research & Studies

What is CJC-1295 (with DAC)?

CJC-1295 (with DAC) is a synthetic tetrasubstituted analog of growth hormone-releasing hormone engineered with a Drug Affinity Complex. The DAC moiety forms a covalent bond with circulating serum albumin, extending the peptide half-life from minutes to multiple days in experimental systems. This property positions the compound as a laboratory tool for examining prolonged GHRH-receptor occupancy. It is supplied exclusively for in-vitro and controlled laboratory research.

Mechanism of Action

In model systems the peptide binds GHRH receptors expressed on somatotroph cells, activating Gs-coupled signaling that elevates cyclic AMP and promotes growth-hormone gene transcription and secretion. Concurrent albumin binding via the DAC group maintains receptor stimulation over extended intervals, producing a continuous rather than episodic GH output. Downstream, the sustained GH elevation drives measurable increases in insulin-like growth factor-1 in the same experimental preparations. Researchers exploit this profile to dissect tonic versus pulsatile endocrine signaling.

Primary Areas of Research

Investigators employ CJC-1295 (with DAC) to map the consequences of uninterrupted GHRH-receptor activation on baseline GH and IGF-1 trajectories across multi-day observation windows. Comparative studies contrast this continuous “GH bleed” pattern with the discrete pulses generated by short-acting GHRH fragments or ghrelin mimetics. Additional work examines receptor desensitization kinetics, second-messenger dynamics, and transcriptional feedback loops under prolonged ligand exposure in cell-culture and isolated-tissue models.

Key Research Findings

Laboratory data confirm that albumin conjugation markedly lengthens circulating residence time relative to unmodified GHRH analogs. Sustained receptor engagement elevates trough GH concentrations and secondary IGF-1 levels for days rather than hours in preclinical preparations. Parallel experiments demonstrate that continuous stimulation produces distinct gene-expression signatures compared with intermittent secretagogue challenge. These observations establish the compound as a reference agent for duration-dependent endocrine pathway analysis.

Research Handling & Considerations

CJC-1295 (with DAC) is intended solely for in-vitro assays and non-clinical laboratory investigation. Standard peptide-handling practices apply: protect from repeated freeze-thaw cycles, reconstitute in appropriate research-grade diluents, and store lyophilized material under desiccated, low-temperature conditions. All experimental designs must remain confined to controlled research environments; the material is not for human or animal consumption.

Frequently Asked Questions

The Drug Affinity Complex enables covalent attachment to serum albumin, thereby extending the peptide’s experimental half-life from minutes to several days and permitting continuous GHRH-receptor stimulation studies.

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