CJC-1295 no DAC 5mg

CJC-1295 without DAC (Drug Affinity Complex) is a short-acting growth hormone-releasing hormone (GHRH) analog known for stimulating natural pulsatile GH release. Unlike the DAC version, this form of CJC-1295 promotes physiologically-timed growth hormone spikes, aligning with the body’s natural rhythms. It is often combined with GHRP peptides like Ipamorelin to maximize GH output, making it highly valuable in research on recovery, fat loss, and anti-aging.

CJC-1295 (No DAC) offers a flexible and physiologically-aligned tool for researchers focused on hormonal optimization, physical recovery, and metabolic health.

Key Benefits:

• Natural GH Pulses: Encourages more physiologic growth hormone release patterns.
• Improved Recovery: Supports tissue regeneration, especially when stacked with GHRPs.
• Fat Loss & Lean Mass Support: Increases GH and IGF-1, aiding fat metabolism and muscle maintenance.
• Sleep & Cellular Repair: Enhances restorative processes typically active during deep sleep.
• Short-Acting Precision: Allows better timing control in GH research protocols.

CJC-1295 without DAC is a synthetic analog of growth hormone-releasing hormone (GHRH), engineered to stimulate the secretion of growth hormone (GH) in non-human research subjects. Unlike its DAC counterpart, this form lacks the Drug Affinity Complex, resulting in a shorter half-life, typically around 30 minutes to a few hours in test subjects. Despite this reduced duration of activity, it effectively binds to GHRH receptors, triggering a cascade of signaling events that enhance pulsatile GH release.

In laboratory studies, CJC-1295 without DAC has demonstrated utility in investigating the GH/IGF-1 axis, protein synthesis, and tissue repair processes. Additionally, this version of the peptide provides insights into receptor-binding kinetics, enzymatic degradation, and short-term effects on cellular metabolism in test subjects.

The absence of DAC allows for a more transient yet targeted approach to studying endocrine function, making it a valuable tool for experiments requiring immediate but time-limited modulation of GH levels in controlled research environments in non-human research subjects.