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Briakinumab CAS NO 339308-60-0
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CAS No.:339308-60-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Briakinumab is a high-purity, fully human monoclonal antibody targeting the p40 subunit of interleukin-12 (IL-12) and interleukin-23 (IL-23). This compound is a critical research and development tool for investigating the pathophysiology and therapeutic modulation of immune-mediated inflammatory diseases. Briakinumab CAS NO 339308-60-0 is primarily utilized by pharmaceutical R&D teams, biotechnology companies, and academic research institutions focused on immunology and autoimmune disorders.
Application
- Biopharmaceutical Research & Development: A key reference standard and active pharmaceutical ingredient (API) in pre-clinical and clinical-stage drug development programs targeting IL-12/IL-23 pathways.
- Immunology Mechanism Studies: Used in in vitro and in vivo models to elucidate the role of IL-12 and IL-23 in autoimmune and chronic inflammatory conditions.
- Therapeutic Antibody Benchmarking: Serves as a critical comparator for the development and characterization of next-generation biologic therapies for psoriasis, psoriatic arthritis, and Crohn's disease.
- Diagnostic Reagent Development: Employed in the development of immunoassays and diagnostic kits to detect and quantify specific cytokines or related biomarkers in biological samples.
- Cell Signaling & Pathway Analysis: A vital tool for studying T-helper cell (Th1 and Th17) differentiation and function in research laboratories.
Basic Information
| Product Name | Briakinumab |
| CAS No. | 339308-60-0 |
| Molecular Formula | C6420H9916N1720O2016S46 |
| Molecular Weight | Approx. 144 kDa |
| Synonyms | ABT-874; Anti-IL-12/IL-23 p40 Monoclonal Antibody; IL-12/IL-23 Inhibitor; Human IgG1κ Monoclonal Antibody (anti-IL12/23p40); Monoclonal Antibody to Interleukin 12, p40 Subunit; Monoclonal Antibody to Interleukin 23, p40 Subunit |
| EINECS | Contact for details |
Quality Control
Our Briakinumab is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical characterization to ensure identity, purity, potency, and consistency. We provide full traceability and Certificates of Analysis (COA) detailing results from orthogonal methods including HPLC, SDS-PAGE, and bioactivity assays. Production adheres to cGMP guidelines where applicable, supporting its use in regulated research and development.
Storage
Preserve in a tightly closed container, protected from light. For long-term stability, store lyophilized material at -20°C or below. Reconstituted solutions should be aliquoted and stored at -80°C to avoid repeated freeze-thaw cycles. This product is hygroscopic (moisture-sensitive).
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white lyophilized powder or clear solution |
| Identification (HPLC/MS) | Conforms to reference standard |
| Purity (SDS-PAGE, reduced & non-reduced) | > 95% |
| Purity (SEC-HPLC) | > 98% Monomer |
| Protein Content (UV Absorbance) | > 1.0 mg/mL (for solutions) |
| Endotoxin Level (LAL) | < 1.0 EU/mg |
| Biological Activity (Cell-based assay) | IC50 as per COA |
| Sterility (Membrane Filtration) | Sterile |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Why choose US
Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






