
CJC-1295 (no DAC) 5MG
$35.00 $29.75
CJC-1295 (no DAC) 5MG · Reference CJCND-PW-5MG
In stock
| # Purchased | Discounted Price |
|---|---|
| 5 - 9 | $33.25 |
| 10 + | $31.50 |
- Product Reference
- CJCND-PW-5MG
- Documentation
- Find This Product’s Reports ↗
About CJC-1295 (no DAC) 5MG
CJC-1295 (no DAC)
CJC-1295 (no DAC) is a research grade synthetic peptide developed for controlled laboratory investigation of growth hormone releasing hormone pathways. This non-DAC format allows research teams to evaluate timing dependent behavior within structured experimental windows. Because it excludes Drug Affinity Complex modification, it is often selected for study designs that prioritize tighter observation intervals, repeatable sampling, and protocol flexibility.
In RUO settings, compound selection depends on consistency, documentation, and reliable handling characteristics. Therefore, CJC-1295 (no DAC) is supplied in a lyophilized format to support stable storage prior to controlled reconstitution. When used within qualified laboratory environments, it fits well into workflows that require precise planning, clear recordkeeping, and repeatable procedures.
Non-DAC Structure for Timing Controlled Research
The “no DAC” designation indicates that this peptide does not include an extended binding modification. As a result, researchers can better align experimental timing with short window data collection, comparative models, and protocol variations. Additionally, this structure supports research designs that focus on pulse style evaluation, time course comparisons, and method development for analytical measurement.
Key Features for Laboratory Workflows
- Synthetic peptide supplied for research use only
- Non-DAC modified structure for timing specific study design
- Lyophilized powder format for controlled reconstitution procedures
- Suitable for structured in vitro evaluation and laboratory investigation
- Produced with quality focused processes appropriate for RUO handling
Research Applications and Protocol Fit
CJC-1295 (no DAC) is commonly integrated into research frameworks where timing, sampling, and comparison are central. For example, laboratories may use it while developing assay methods, evaluating pathway responses, or comparing non-DAC and DAC style formats under consistent conditions. Because timing variables can materially impact study outcomes, the non-DAC structure can help align observation windows with planned collection points and analytical readouts.
Moreover, the lyophilized presentation supports inventory control and lab routine standardization. This can simplify preparation steps when teams follow validated procedures for labeling, documentation, and controlled reconstitution. Consequently, researchers can maintain consistent handling practices across multiple runs and protocol iterations.
Handling and Storage Notes
Store CJC-1295 (no DAC) in a cool, dry environment prior to reconstitution. After reconstitution, follow standard laboratory storage protocols based on your internal procedures and study requirements. Always use proper sterile technique, calibrated equipment, and appropriate documentation for each preparation step. For best consistency, maintain a controlled workflow that includes lot tra
Product. Strength. Lot.
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- Catalog Name
- CJC-1295 (no DAC) 5MG
- Product Reference
- CJCND-PW-5MG
- Intended Use
- Laboratory research only
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Contact supportFrequently Asked Questions
CJC-1295 (no DAC) binds to GHRH receptors on somatotroph cells in the anterior pituitary, triggering intracellular signaling such as increased cyclic AMP (cAMP) that promotes endogenous growth hormone releaser pathways in research models. This receptor interaction is similar to that of endogenous GHRH but without extended systemic retention.
Without the Drug Affinity Complex (DAC), CJC-1295 (no DAC) has a shorter half-life in experimental systems compared with the DAC-modified version. This results in more pulsatile receptor activation rather than prolonged receptor engagement, which is useful in research contexts where shorter signaling bursts are studied.
Activation of the GHRH receptor by CJC-1295 (no DAC) initiates downstream pathways including cAMP/PKA signaling and subsequent peptide-linked hormone axis events. These signaling events influence patterns of growth hormone axis activity and insulin-like growth factor 1 (IGF-1) signaling in controlled research settings.
CJC-1295 (no DAC) is used in in vitro and animal studies to analyze receptor pharmacology, hormone axis activation, and gene expression changes linked to growth hormone regulator pathways. Its short signaling profile makes it a useful tool for studies of pulsatile endocrine dynamics.
CJC-1295 (no DAC) binds to GHRH receptors on somatotroph cells in the anterior pituitary, triggering intracellular signaling such as increased cyclic AMP (cAMP) that promotes endogenous growth hormone releaser pathways in research models. This receptor interaction is similar to that of endogenous GHRH but without extended systemic retention.
CJC-1295 (no DAC) is studied because its precise peptide sequence and receptor target allow researchers to dissect how growth hormone releaser signaling influences downstream biochemical networks. Its defined receptor interaction provides insight into endocrine signaling mechanisms and intracellular pathways tied to peptide-mediated hormone axis regulation.
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