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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG4, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Evunzekibart Biosimilar - Anti-CD137 mAb - Research Grade |
|---|---|
| Species | Homo sapiens |
| Expression system | XtenCHO |
| Purity | >90% by SDS-PAGE. |
| Buffer | 0.01M PBS, pH 7.4. |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | 4°C for short term; -20°C for long term |
| Brand | ProteoGenix |
| Aliases /Synonyms | anti-CD137, Tumor necrosis factor receptor superfamily member 9, 4-1BB ligand receptor, CDw137, TNFRSF9, T-cell antigen ILA, T-cell antigen 4-1BB homolog, ILA |
| Reference | PX-TA2064 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Evunzekibart Biosimilar is a research grade anti-CD137 monoclonal antibody (mAb) that has been developed as a potential therapeutic agent for various diseases. In this article, we will delve into the structure, activity, and potential applications of this biosimilar in the field of antibody-based therapeutics.
Evunzekibart Biosimilar is a fully humanized monoclonal antibody, also known as Evunzekibart mAb, that targets the CD137 protein. It is composed of two identical heavy chains and two identical light chains, with a molecular weight of approximately 150 kDa. The antibody has a Y-shaped structure, with two antigen-binding fragments (Fab) and one crystallizable fragment (Fc) region. The Fab region is responsible for binding to the CD137 protein, while the Fc region mediates effector functions such as antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC).
The main target of Evunzekibart Biosimilar is the CD137 protein, also known as 4-1BB, which is a member of the tumor necrosis factor receptor (TNFR) superfamily. CD137 is expressed on the surface of various immune cells, including T cells, B cells, natural killer (NK) cells, and dendritic cells. Upon binding to CD137, Evunzekibart mAb activates the CD137 signaling pathway, leading to the activation and proliferation of immune cells. This results in an enhanced immune response against cancer cells and infectious agents.
In addition to its direct effects on immune cells, Evunzekibart Biosimilar also has an indirect anti-tumor activity. The Fc region of the antibody can bind to Fc receptors on immune cells, triggering ADCC and CDC mechanisms. This leads to the destruction of cancer cells by immune cells, further enhancing the anti-tumor effect of Evunzekibart mAb.
As a research grade anti-CD137 mAb, Evunzekibart Biosimilar has shown promising results in preclinical studies for the treatment of various diseases. Its main therapeutic target is cancer, particularly solid tumors. The activation of the CD137 signaling pathway by Evunzekibart mAb has been shown to inhibit tumor growth and promote tumor regression in animal models.
In addition to cancer, Evunzekibart Biosimilar has also shown potential in the treatment of infectious diseases. By activating the immune response, the antibody can enhance the body’s ability to fight against viral and bacterial infections. This has been demonstrated in preclinical studies for diseases such as HIV, influenza, and tuberculosis.
Furthermore, Evunzekibart Biosimilar has been investigated for its potential use in autoimmune diseases. The CD137 signaling pathway has been implicated in the pathogenesis of autoimmune disorders, and Evunzekibart mAb has shown to inhibit this pathway, leading to a decrease in disease severity in animal models.
In summary, Evunzekibart Biosimilar is a research grade anti-CD137 mAb with a well-defined structure and potent activity against its therapeutic target. Its potential applications in cancer, infectious diseases, and autoimmune disorders make it a promising candidate for further development as a therapeutic agent. Further clinical studies are needed to fully evaluate the safety and efficacy of Evunzekibart mAb in humans, but the preclinical data is highly encouraging.
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