Laboratory researchers seeking to buy CJC-1295 without DAC select this tetrasubstituted 29-amino acid growth hormone-releasing hormone (GHRH) analog—also known as Mod GRF 1-29—to evaluate pulsatile GH and downstream IGF-1 secretion in vitro and in animal models. PX1 Research supplies USA-manufactured CJC-1295 without DAC at >99% purity, verified via lot-specific RP-HPLC and mass spectrometry.
Laboratory researchers seeking to buy CJC-1295 without DAC select this tetrasubstituted 29-amino acid growth hormone-releasing hormone (GHRH) analog—also known as Mod GRF 1-29—to evaluate pulsatile GH and downstream IGF-1 secretion in vitro and in animal models. PX1 Research supplies USA-manufactured CJC-1295 without DAC at >99% purity, verified via lot-specific RP-HPLC and mass spectrometry.
CJC-1295 without DAC, chemically designated as Modified GRF 1-29 (Mod GRF 1-29), is a synthetic peptide analog of endogenous growth hormone-releasing hormone (GHRH). Natural GHRH consists of 44 amino acids, but bioactivity resides entirely within the N-terminal 29-amino-acid chain known as GRF 1-29 (sermorelin). To overcome the rapid enzymatic degradation of native GRF 1-29 by dipeptidyl peptidase-IV (DPP-IV), researchers engineered four specific amino acid substitutions at positions 2, 8, 15, and 27.
The resulting tetrasubstituted peptide 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—exhibits significantly enhanced metabolic stability against plasma proteases. When investigators choose to buy CJC-1295 without DAC, they obtain a compound that mimics natural physiological GHRH release patterns without the covalent albumin-binding complex attached to the Drug Affinity Complex (DAC) variant.
In physiological and analytical settings, this molecular configuration allows researchers to observe acute, concentration-dependent receptor activation. Understanding these structural modifications is essential when evaluating peptide interactions within our broader catalog of research peptides.
CJC-1295 without DAC functions as a selective agonist at the growth hormone-releasing hormone receptor (GHRH-R), a G-protein-coupled receptor located on pituitary somatotropes. Upon receptor binding, Mod GRF 1-29 stimulates the Gαs subunit, activating adenylate cyclase and increasing intracellular cyclic adenosine monophosphate (cAMP). This signaling cascade triggers protein kinase A (PKA) activation, opening voltage-gated calcium channels and stimulating the exocytosis of stored growth hormone granules.
Unlike its long-acting counterpart containing the Drug Affinity Complex, CJC-1295 without DAC demonstrates an in vivo plasma half-life of approximately 30 minutes in rodent and mammalian models. This brief half-life preserves natural pulsatile GH release without inducing continuous, non-physiological receptor saturation. Preclinical data indicate that this pulsatile signaling promotes hepatic production of insulin-like growth factor 1 (IGF-1) while preserving endogenous receptor sensitivity.
Investigators interested in mapping downstream somatotrope signaling or cellular transcription dynamics can consult experimental literature within the PX1 Research library, where signaling profiles of various growth hormone secretagogues are documented.
In vitro and animal models show that CJC-1295 without DAC plays a pivotal role in studying tissue regeneration, cellular proliferation, and extracellular matrix remodeling. By elevating transient GH pulses, the peptide accelerates downstream IGF-1 gene expression across muscle satellite cells, chondrocytes, and osteoblasts. Preclinical studies suggest that this cascade supports nitrogen retention and collagen synthesis in damaged connective tissue.
Research in rodent models demonstrates that transient GH pulses induced by Mod GRF 1-29 enhance satellite cell activation following mechanical microtrauma. Furthermore, cellular assays demonstrate upregulation of skeletal muscle protein synthesis via the Akt/mTOR signaling pathway. These properties make the peptide a core tool for investigating acute metabolic recovery, wound healing, and musculoskeletal repair.
In experimental models examining systemic tissue synthesis, investigators often evaluate CJC-1295 without DAC alongside tissue-protective compounds like BPC-157 or extracellular matrix regulators to observe potential synergism in cellular migration and extracellular matrix deposition.
When evaluating GHRH analogs and secretagogues, laboratory researchers must distinguish between short-acting and long-acting configurations. The core distinction between CJC-1295 without DAC and CJC-1295 with DAC lies in the presence of the maleimidopropionic acid linker. To learn more about how these kinetic profiles alter pituitary receptor desensitization, review our technical breakdown on CJC-1295 with DAC vs without DAC.
While CJC-1295 without DAC activates the GHRH pathway directly, growth hormone secretagogue receptor (GHSR-1a) agonists act via a distinct, complementary mechanism. For instance, pairing a GHRH agonist with a selective ghrelin mimetic such as Ipamorelin or GHRP-2 produces a synergistic elevation in GH release in vitro. Alternatively, native Sermorelin represents the unmodified 29-amino-acid chain, which lacks the four stabilizing amino acid substitutions present in Mod GRF 1-29.
The table below outlines key biochemical differences across these preclinical secretagogues:
When sourcing reagents for sensitive assay protocols, verifying purity and manufacturer standards is essential. Prior to selecting CJC 1295 without DAC for sale, procurement officers and principal investigators should verify that the product meets stringent analytical benchmarks to eliminate experimental variability.
PX1 Research enforces rigorous quality assurance metrics across every synthesis lot, including:
• Purity Verification: High-Performance Liquid Chromatography (RP-HPLC) ensuring >99% chemical purity. • Identity Confirmation: Mass Spectrometry (ESI-MS) confirming exact molecular weight (3367.97 Da). • Endotoxin Testing: Kinetic Chromogenic LAL assay ensuring endotoxin levels below 0.01 EU/mg. • Domestic Synthesis: USA-manufactured under ISO 17025 and GMP-compliant conditions. • Lot Traceability: Certificate of Analysis (COA) provided with every vial.
Low-grade or unverified peptides often contain truncated sequences, trifluoroacetate (TFA) salt residues, or bacterial endotoxins that can contaminate cell cultures, induce cytotoxicity, or distort receptor binding kinetics. Sourcing from a verified laboratory partner ensures consistent baseline performance.
Reconstitution of CJC-1295 without DAC must be performed under aseptic conditions within a laminar flow hood to maintain sterile integrity. Lyophilized cake should be dissolved using sterile Bacteriostatic Water (0.9% benzyl alcohol) or Sterile Normal Saline (0.9% NaCl), depending on downstream application requirements.
To reconstitute the peptide correctly in a laboratory setting: 1. Sanitize the rubber stopper of the vial with a 70% isopropyl alcohol swab. 2. Direct the diluent stream gently against the glass wall of the vial rather than directly onto the lyophilized powder. 3. Swirl the vial gently with a slow rotational movement until complete dissolution occurs. Never shake or vortex the vial, as mechanical shear stress can cause peptide denaturation or aggregation. 4. Allow the solution to settle for 2–3 minutes until visual clarity is established.
For cell culture assays sensitive to benzyl alcohol, sterile water for injection (WFI) or phosphate-buffered saline (PBS, pH 7.4) should be utilized immediately prior to application.
Lyophilized CJC-1295 without DAC exhibits high thermal stability when stored under controlled environmental conditions. For long-term shelf storage prior to reconstitution, store lyophilized vials at -20°C to -80°C, protected from light and moisture. Under these conditions, the peptide remains stable for up to 24 months without significant degradation.
Once reconstituted in bacteriostatic water, the peptide solution should be stored at 2°C to 8°C (36°F to 46°F) and utilized within 30 days. Avoid repeated freeze-thaw cycles of reconstituted liquid, as phase transitions induce structural cleavage and peptide aggregation. If aliquoting is required for extended preclinical trial schedules, freeze reconstituted sub-aliquots once at -80°C and thaw immediately prior to use.
PX1 Research is dedicated to providing accredited academic, corporate, and private research laboratories with high-purity reagents. When researchers choose to buy CJC 1295 without DAC through PX1, every order is backed by full analytical transparency, batch-specific COAs, and dedicated customer support.
Orders placed Monday through Friday before 3:00 PM EST ship same-day from our primary distribution hubs in California and Arizona, minimizing transit times and thermal exposure. Institutions needing bulk quantities or custom packaging can apply for a wholesale laboratory account to access volume pricing and dedicated account management.
Where can I buy CJC-1295 without DAC for laboratory research?
You can buy CJC-1295 without DAC directly from PX1 Research. We supply USA-manufactured, HPLC-verified Mod GRF 1-29 for in vitro and preclinical laboratory research, complete with lot-specific Certificates of Analysis.
What is the difference when looking to buy CJC-1295 no-dac mod GRF 1-29 versus CJC-1295 with DAC?
CJC-1295 no-dac (Mod GRF 1-29) lacks the Drug Affinity Complex (DAC) reactive group. This results in a shorter half-life of ~30 minutes, producing rapid, pulsatile GH release. CJC-1295 with DAC contains a maleimide linker that binds serum albumin, extending its half-life to 6–8 days and causing continuous GH elevation.
Why search for CJC 1295 without DAC for sale from USA-based suppliers?
Sourcing CJC 1295 without DAC for sale from domestic USA suppliers guarantees strict quality control under ISO 17025 and GMP-compliant conditions, rapid delivery from CA and AZ fulfillment centers, and protection against degradation associated with international transit times.
How do I verify the purity when deciding to buy CJC 1295 without DAC?
Always request a lot-specific Certificate of Analysis featuring Reverse-Phase High-Performance Liquid Chromatography (RP-HPLC) and Electrospray Ionization Mass Spectrometry (ESI-MS). PX1 Research guarantees purity levels exceeding 99% for every batch.
What is the half-life of Mod GRF 1-29 in preclinical research models?
In animal models and preclinical kinetic evaluations, Mod GRF 1-29 (CJC-1295 without DAC) demonstrates a biological plasma half-life of approximately 30 minutes due to its four protective amino acid substitutions.
How should CJC-1295 without DAC be reconstituted for in vitro assays?
Reconstitute using sterile bacteriostatic water or sterile normal saline under aseptic conditions. Gently trickle the liquid down the inner glass wall of the vial and swirl slowly. Do not shake or vortex the vial.
What endotoxin limits are enforced for CJC-1295 without DAC?
PX1 Research verifies that all lots of CJC-1295 without DAC contain endotoxin levels below 0.01 EU/mg, as measured by kinetic LAL assays, preventing cytotoxic interference in sensitive cell culture models.
Can CJC-1295 without DAC be combined with GHRPs in research protocols?
Yes, in preclinical protocols, GHRH analogs like Mod GRF 1-29 are frequently studied alongside GHRPs (such as Ipamorelin or GHRP-2) to evaluate synergistic GH release triggered by simultaneous activation of GHRH-R and GHSR-1a pathways.
How long does reconstituted CJC-1295 without DAC remain stable at 4°C?
When reconstituted with bacteriostatic water containing 0.9% benzyl alcohol, the solution remains stable for up to 30 days when stored at 2°C to 8°C (36°F to 46°F).
Does PX1 Research offer bulk institutional pricing for CJC-1295 without DAC?
Yes, accredited academic institutions, private laboratories, and corporate research departments can apply for a wholesale laboratory account to receive volume pricing and dedicated logistics support.
All products are sold strictly for laboratory and research use only. Not for human or veterinary use, diagnosis, treatment or consumption. Statements have not been evaluated by the FDA.