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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Quavonlimab Biosimilar - Anti-CTLA4 mAb - Research Grade |
|---|---|
| Source | CAS 2254059-25-9 |
| Species | Humanized |
| Purity | >85% |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3 week if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Quavonlimab,IMMUNOGLOBULIN G1, ANTI-(HUMAN CYTOTOXIC T-LYMPHOCYTE-ASSOCIATED ANTIGEN 4) (HUMAN-MUS MUSCULUS MONOCLONAL M3 .GAMMA.1-CHAIN), DISULFIDE WITH HUMAN-MUS MUSCULUS MONOCLONAL M3 .KAPPA.-CHAIN, DIMER, IMMUNOGLOBULIN G1-KAPPA, ANTI-(HOMO SAPIENS CTLA4 (CYTOTOXIC T-LYMPHOCYTE-ASSOCIATED PROTEIN 4, CD152)), HUMANIZED MONOCLONAL ANTIBODY,MK-1308A,CTLA4,anti-CTLA4 |
| Reference | PX-TA1707 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1,Kappa |
| Clonality | Monoclonal Antibody |
Quavonlimab Biosimilar, also known as Anti-CTLA4 mAb, is a research grade monoclonal antibody that has been developed as a biosimilar to the original drug, Ipilimumab. It is a humanized IgG1 antibody that specifically targets the cytotoxic T-lymphocyte-associated protein 4 (CTLA4) receptor. This protein is a negative regulator of T-cell activation and plays a critical role in immune regulation. By blocking the activity of CTLA4, Quavonlimab Biosimilar enhances the anti-tumor immune response and has potential therapeutic applications in various cancers.
Quavonlimab Biosimilar is a recombinant antibody that is produced in Chinese Hamster Ovary (CHO) cells. It is composed of two identical heavy chains and two identical light chains, linked by disulfide bonds. The heavy chain consists of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chain consists of two constant domains (CL and CL’) and one variable domain (VL). The variable domains of both the heavy and light chains form the antigen-binding site, which specifically recognizes and binds to CTLA4.
Quavonlimab Biosimilar works by binding to CTLA4 on the surface of T-cells, blocking its interaction with its ligands, CD80 and CD86. This prevents the inhibitory signal from being transmitted, leading to increased T-cell activation and proliferation. Additionally, Quavonlimab Biosimilar also promotes the activation of effector T-cells and inhibits the activity of regulatory T-cells, further enhancing the anti-tumor immune response.
Quavonlimab Biosimilar has shown promising results in preclinical and clinical studies for the treatment of various cancers. It has been approved by the FDA for the treatment of advanced melanoma and is currently being investigated for its potential in other types of cancer, such as lung cancer, bladder cancer, and renal cell carcinoma. In combination with other immunotherapies, Quavonlimab Biosimilar has also shown efficacy in treating resistant or relapsed cancers.
Compared to the original drug, Ipilimumab, Quavonlimab Biosimilar has several advantages. Firstly, it is a biosimilar, meaning it has a highly similar structure and function to the original drug, making it a more affordable option for patients. Additionally, Quavonlimab Biosimilar has a longer half-life, allowing for less frequent dosing. It also has a lower risk of immune-related adverse events, making it a safer option for patients.
Quavonlimab Biosimilar is a promising research grade antibody that specifically targets CTLA4 and has potential therapeutic applications in various cancers. Its unique mechanism of action and advantages over the original drug make it a valuable addition to the arsenal of cancer treatments. Further research and clinical trials are needed to fully understand the potential of Quavonlimab Biosimilar in improving patient outcomes and survival rates.
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