CJC-1295 BioStrips
CJC-1295 BioStrips view 1
CJC-1295 BioStrips view 2
Peptide Capsules
Verified Quality

CJC-1295 BioStrips

4.88 (34 Reviews)
Ships worldwide
$199.97

Sales Tax included at checkout

Laboratory Research Chemical • Scroll down for full specifications

1

Priority Shipping

Fast & Discreet

99% Purity

HPLC Verified

Full Refund

60-Day Promise

Lab Synthesis

GMP Certified

Product Information

Detailed laboratory specifications, compound structure, and research applications.

Research Grade

HPLC 99%+ Purity

Verified Origin

GMP Manufactured

CJC-1295 Product Description

CJC-1295 is a modified version of GHRH (1-29), the shortest fragment of GHRH, a 44-amino-acid peptide produced in the hypothalamus. CJC-1295 binds to GHRHR on somatotroph cells in the anterior pituitary with high affinity, mimicking GHRH’s action. This binding activates the GHRHR, initiating intracellular signaling cascades.

Contains 20 buccal strips (150mcg) for research purposes.

CJC-1295 Peptide Structure

Molecular Formula: C152H252N44O42

Molecular Mass: 3367.9 g/mol

Pubchem CID: 56841945

Synonyms:

  • 863288-34-0
  • CJC-1295 No DAC

Research Areas:

  • Albumin Binding
  • IGF-1 Elevation
  • Growth Hormone Pathways

CJC-1295 Research

CJC-1295, also known as Modified GRF 1-29, is a synthetic analog of growth hormone-releasing hormone (GHRH) that offers unique research opportunities for laboratories studying growth hormone pathways. The compound’s distinctive albumin-binding characteristics provide researchers with extended observation windows for mechanism studies.

Albumin Binding Mechanism

The primary research interest in CJC-1295 centers on its ability to form stable conjugates with serum albumin through its reactive maleimidopropionic acid group. This bioconjugation mechanism creates covalent bonds with free thiols on plasma proteins, offering researchers a model for studying protein-peptide interactions[1].

Laboratory studies demonstrate this binding strategy extends the compound’s detectable presence in circulation beyond 72 hours. This contrasts significantly with native GHRH’s very short detection window[2]. Research teams can leverage this extended timeframe for pharmacokinetic studies and mechanism investigations.

Growth Hormone Pathway

CJC-1295 functions as a selective GHRH analog that provides researchers with tools for studying anterior pituitary stimulation pathways. Laboratory investigations show the compound maintains natural pulsatile secretion patterns while allowing detailed observation of growth hormone release mechanisms[3].

Research data indicates a 4-fold increase in growth hormone area under the curve over 2-hour observation periods compared with native hGRF(1-29)[2]. Studies also demonstrate the peptide’s ability to increase basal growth hormone levels by 7.5-fold while preserving natural pulsatility patterns[3].

These findings offer research teams validated endpoints for studying growth hormone regulation and pituitary function in laboratory models.

Growth Hormone Deficiency

Preclinical research using GHRH knockout mouse models provides laboratories with established methodologies for studying growth hormone pathway restoration. Research demonstrates that once-daily administration protocols can normalize growth parameters, body weight, and length measurements in these models[4].

Laboratory investigations show the compound stimulates somatotroph cell proliferation and increases total pituitary RNA and GH mRNA expression. These findings suggest researchers can study pituitary function restoration in models with intact secretory capability but deficient GHRH signaling[4].

This research framework offers laboratories clear protocols for investigating growth hormone pathway interventions and measuring functional outcomes.

IGF-1 Research

Laboratory studies consistently demonstrate CJC-1295’s effects on insulin-like growth factor-1 (IGF-1) levels, providing researchers with measurable biomarkers. Research data shows mean plasma IGF-1 concentrations increase 1.5- to 3-fold for 9-11 days following single administration in study models[5].

Multiple administration studies reveal mean IGF-1 levels remain elevated above baseline for up to 28 days[5]. This sustained elevation offers research teams extended observation windows for studying IGF-1’s role in mediating growth hormone effects[3].

These findings provide laboratories with validated biomarkers and timeframes for investigating growth hormone downstream signaling pathways.

Research Methodologies and Applications

Laboratory Study Opportunities:

  • Pharmacokinetic Studies – Extended half-life enables detailed absorption and distribution research
  • Mechanism Investigations – Albumin binding provides models for protein-peptide interaction studies
  • Biomarker Research – IGF-1 elevation offers measurable endpoints for pathway studies
  • Pituitary Function Studies – Cell proliferation effects enable organoid and tissue culture research

Research Models:

  • In vitro pituitary cell culture systems
  • Ex vivo tissue preparation studies
  • Animal model investigations with established protocols
  • Bioconjugation mechanism studies

Research Considerations

Laboratories investigating CJC-1295 benefit from its well-characterized pharmacokinetic profile and established research methodologies. The compound’s albumin binding mechanism offers unique opportunities for studying bioconjugation strategies and extended-release peptide design.

Research teams should note the compound’s selective GHRH receptor activity and preserved pulsatile patterns when designing experimental protocols. The sustained IGF-1 elevation provides reliable biomarkers for mechanism studies and pathway investigations.

References:

  1. Timms, M., Bailey, S., Steel, R., Forbes, G., & Ganio, K. (2018). An immuno polymerase chain reaction screen for the detection of CJC-1295 and other growth-hormone-releasing hormone analogs in equine plasma. Drug testing and analysis, 11 6, 804-812. https://doi.org/10.1002/dta.2554.
  2. Robitaille, M., Pham, K., Pellerin, I., Bridon, D., Benquet, C., Jetté, L., Paradis, V., Léger, R., Thibaudeau, K., & Van Wyk, P. (2005). Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats: identification of CJC-1295 as a long-lasting GRF analog. Endocrinology, 146 7, 3052-8. https://doi.org/10.1210/EN.2004-1286.
  3. Ionescu, M., & Frohman, L. (2006). Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog. The Journal of clinical endocrinology and metabolism, 91 12, 4792-7. https://doi.org/10.1210/JC.2006-1702.
  4. Alba, M., Castaigne, J., Fintini, D., Salvatori, R., Lawrence, B., Frohman, L., & Sagazio, A. (2006). Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse. American journal of physiology. Endocrinology and metabolism, 291 6, E1290-4. https://doi.org/10.1152/AJPENDO.00201.2006.
  5. Gagnon, C., Lawrence, B., Frohman, L., Teichman, S., Castaigne, J., & Neale, A. (2006). Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults. The Journal of clinical endocrinology and metabolism, 91 3, 799-805. https://doi.org/10.1210/JC.2005-1536.

Research Chemical Disclaimer

This product is intended for laboratory research use only. It is not for human consumption, diagnostic, or therapeutic purposes. Handling should only be performed by qualified professionals.

Complete Your Research

Synergistic compounds from the Peptide Capsules lineup

View Full Collection
MicroFLGR (2MG)

MicroFLGR (2MG)

Product Description

Follistatin (FLGR242), is a novel fragmented, modified version of Follistatin-344 (FST-344) that does not bind to the protein activin. Activin is responsible for the negative effects of myostatin inhibition such as unwanted cellular growth in laboratory models. It also contains a patented albumin binder.

Follistatin protein (FST) fused with an albumin-binding construct that uses a hydrophilic glycine-serine linker to achieve high-affinity binding to serum albumin (<20 nM Kd). This recombinant technology allows researchers to study follistatin-albumin interactions and protein trafficking in experimental systems.

Research applications include muscle mass development studies, activin neutralization assays, and TGF-β superfamily pathway modulation with albumin binding dynamics. The construct maintains biological activity while enabling investigation of albumin as a carrier protein.

US GMP-manufactured with third-party verification and comprehensive COAs for reproducible research outcomes.

Peptide Information

Property Value
Peptide Type Follistatin-Albumin Binding Construct
Technology Albumin-binding peptide fusion (GGSGGSGGSGGRLIEDICLPRWGCLWEDD linker)
Molecular Weight ~40 kDa
Binding Affinity <20 nM
Synonyms FST-Albumin Construct, Extended Half-Life Follistatin

Lyophilized Peptides:

These peptides are freeze-dried, a process that not only extends shelf life but also preserves the purity and integrity of the peptides during storage. We do not use any fillers in this process.

Product Usage:

This PRODUCT IS INTENDED AS A RESEARCH CHEMICAL ONLY. This designation allows the use of research chemicals strictly for in vitro testing and laboratory experimentation only. All product information available on this website is for educational purposes only.  This product should only be handled by licensed, qualified professionals. This product is not a drug, food, or cosmetic and may not be misbranded, misused or mislabeled as a drug.

$15000.00

Follistatin (FLGR242) (10mg)
Options

Follistatin (FLGR242) (10mg)

Product Description

Follistatin (FLGR242), is a novel fragmented, modified version of Follistatin-344 (FST-344) that does not bind to the protein activin. Activin is responsible for the negative effects of myostatin inhibition such as unwanted cellular growth in laboratory models. It also contains a patented albumin binder.

Follistatin protein (FST) fused with an albumin-binding construct that uses a hydrophilic glycine-serine linker to achieve high-affinity binding to serum albumin (<20 nM Kd). This recombinant technology allows researchers to study follistatin-albumin interactions and protein trafficking in experimental systems.

Research applications include muscle mass development studies, activin neutralization assays, and TGF-β superfamily pathway modulation with albumin binding dynamics. The construct maintains biological activity while enabling investigation of albumin as a carrier protein.

US GMP-manufactured with third-party verification and comprehensive COAs for reproducible research outcomes.

Peptide Information

Property Value
Peptide Type Follistatin-Albumin Binding Construct
Technology Albumin-binding peptide fusion (GGSGGSGGSGGRLIEDICLPRWGCLWEDD linker)
Molecular Weight ~40 kDa
Binding Affinity <20 nM
Synonyms FST-Albumin Construct, Extended Half-Life Follistatin

Lyophilized Peptides:

These peptides are freeze-dried, a process that not only extends shelf life but also preserves the purity and integrity of the peptides during storage. We do not use any fillers in this process.

Product Usage:

This PRODUCT IS INTENDED AS A RESEARCH CHEMICAL ONLY. This designation allows the use of research chemicals strictly for in vitro testing and laboratory experimentation only. All product information available on this website is for educational purposes only.  This product should only be handled by licensed, qualified professionals. This product is not a drug, food, or cosmetic and may not be misbranded, misused or mislabeled as a drug.

$2397 – $28764

Klotho (alphaKlothoLR) (20mcg)
Options

Klotho (alphaKlothoLR) (20mcg)

Product Description

alphaKlothoLR is a patented, long-release version of the recombinant Klotho protein, which contains specific amino acid sequences, linkers, and an albumin binding group that allows for a sustained delivery of Klotho with cellular activity up to 19 days.

This research-grade construct combines α-Klotho protein with a proprietary 29-amino acid albumin binding peptide (GGSGGSGGSGGRLIEDICLPRWGCLWEDD). The modification enables strong albumin binding affinity (<20 nM) while maintaining native FGF23 binding activity (15-30 nM).

Produced through recombinant expression with rigorous third-party testing. Each batch includes HPLC and LC-MS verification to confirm molecular identity and purity standards. Complete analytical documentation supports laboratory applications investigating protein-albumin interactions, FGF23 signaling pathways, and albumin binding mechanisms.

For in vitro research use only.

Klotho Protein Information

Property Value
Peptide Sequence α-Klotho protein (1012 amino acids) + albumin binding construct: GGSGGSGGSGGRLIEDICLPRWGCLWEDD
Molecular Weight ~133-135 kDa (full construct with albumin binder)
Albumin Binding Affinity (Kd) <20 nM
FGF23 Binding Affinity (Kd) 15-30 nM (optimized: 16.2 nM)
Synonyms α-Klotho-albumin binding construct, Modified Klotho with glycine-serine linker

Lyophilized Peptides:

These peptides are freeze-dried, a process that not only extends shelf life but also preserves the purity and integrity of the peptides during storage. We do not use any fillers in this process.

Product Usage:

This PRODUCT IS INTENDED AS A RESEARCH CHEMICAL ONLY. This designation allows the use of research chemicals strictly for in vitro testing and laboratory experimentation only. All product information available on this website is for educational purposes only.  This product should only be handled by licensed, qualified professionals. This product is not a drug, food, or cosmetic and may not be misbranded, misused or mislabeled as a drug.

$2397 – $15341

Research Specification

Comprehensive documentation for laboratory application and compound verification.

HPLC Verification

Purity levels exceeding 99.2% guaranteed via third-party high-performance liquid chromatography testing.

Storage Compliance

Stored at -20°C in oxygen-free environment. Shipped with cold-chain monitoring protocols.

CAS Registry

Uniquely identified compound with full structural validation and mass spectrometry reports.

Usage Policy

Strictly for lab research. Not for human or therapeutic use. Waiver required for bulk orders.