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CJC-1295 with DAC

Endocrine signaling research

CJC-1295 with DAC

Lyophilized endocrine-signaling research peptide for systems review

CJC-1295 with DAC is a longer-acting GHRH analog studied for extended GH-axis signaling and albumin-binding pharmacology.

Price range: 49.99 $ through 212.99 $
98.6%-99.2% Lyophilized powder 5 mg
Available documentation

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For laboratory research use only. Not for human or veterinary use. Not intended to diagnose, treat, cure, mitigate, or prevent disease.

Storage

Keep sealed, cold, dry, and protected from heat swings. Confirm product-specific storage on arrival.

Shipping notes

Packed for transit stability with order support available for warm-weather routes.

Batch reference

Batch-linked certificate support is available through the documentation desk.

Research context

CJC-1295 with DAC research profile

CJC-1295 with DAC is a longer-acting GHRH analog designed to extend exposure through drug-affinity-complex chemistry and albumin binding. Research examines pharmacokinetics, prolonged GH and IGF-1 marker changes, pituitary signaling, and how sustained activity differs from shorter GHRH analogs. It is distinct from CJC-1295 No DAC, which is used for shorter pulse-pattern comparisons, and from ipamorelin or GHRP compounds, which signal through the ghrelin receptor. This version is most relevant when half-life extension is central to the study design. Published pharmacology for named investigational material does not independently verify the sequence, purity, or performance of a catalog batch.

Proposed mechanism

A GHRH analog containing a drug-affinity-complex group designed to form a covalent bond with serum albumin. Albumin binding reduces clearance and prolongs GHRH-receptor stimulation, increasing GH secretion and downstream IGF-1.

Effects reported in studies

  • Healthy-adult studies reported dose-dependent increases in GH lasting several days and increases in IGF-1 lasting approximately one to two weeks after studied exposures.
  • Repeated exposure in pharmacology studies produced sustained elevation of GH and IGF-1 without eliminating pulsatile secretion.
  • Reported observations included injection-site reactions and endocrine changes expected from prolonged GH-axis stimulation.

Common research endpoints

Albumin binding, half-life, GHRH receptor activity, GH pulse pattern, integrated GH exposure, IGF-1, glucose, insulin, binding proteins, pharmacokinetics, and adverse events.

Evidence and limitations

Controlled human pharmacology exists for the original investigational CJC-1295 with DAC. Product sequence and DAC chemistry must match before those data are considered relevant.

External reading

Literature for context—not product proof.

Third-party sources describe their own research materials and methods. They do not validate a specific Azure catalog batch.

Support and documentation

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