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| Size | 100µg, 1MG |
|---|---|
| Isotype | IgG4;G4 Kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Linvoseltamab Biosimilar - Anti-TNFRSF17 mAb - Research Grade |
|---|---|
| Species | Bispecific Homo Sapiens |
| Expression system | XtenCHO |
| 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 | Linvoseltamab,,TNFRSF17,anti-TNFRSF17 |
| Reference | PX-TA1859 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4;G4 Kappa |
| Clonality | Monoclonal Antibody |
Linvoseltamab Biosimilar, also known as Anti-TNFRSF17 mAb, is a research grade monoclonal antibody that has shown promising results in the treatment of various diseases. This article aims to provide a comprehensive scientific description of the structure, activity, and potential applications of this biosimilar.
Linvoseltamab Biosimilar is a humanized monoclonal antibody that specifically targets the tumor necrosis factor receptor superfamily member 17 (TNFRSF17), also known as B-cell maturation antigen (BCMA). It is composed of two heavy chains and two light chains, each containing variable and constant regions. The variable regions are responsible for binding to TNFRSF17, while the constant regions determine the antibody’s effector functions.
Linvoseltamab Biosimilar works by binding to TNFRSF17, which is highly expressed on the surface of malignant plasma cells in multiple myeloma and other B-cell malignancies. This binding inhibits the interaction between TNFRSF17 and its ligands, BAFF and APRIL, leading to the inhibition of B-cell survival and proliferation. Additionally, Linvoseltamab Biosimilar also triggers antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) against TNFRSF17-expressing cells, further enhancing its anti-tumor activity.
Linvoseltamab Biosimilar has shown promising results in preclinical and clinical studies for the treatment of multiple myeloma and other B-cell malignancies. In a phase 1 clinical trial, it demonstrated significant anti-tumor activity in patients with relapsed or refractory multiple myeloma, with an overall response rate of 60%. It has also shown potential in combination therapy with other anti- cancer agents, such as lenalidomide and dexamethasone, in both preclinical and clinical studies.
In addition to its use in cancer treatment, Linvoseltamab Biosimilar has also shown potential in the treatment of autoimmune diseases. TNFRSF17 is involved in the pathogenesis of autoimmune diseases, such as systemic lupus erythematosus and rheumatoid arthritis, making it a promising therapeutic target. Preclinical studies have shown that Linvoseltamab Biosimilar can effectively inhibit the activity of TNFRSF17 and ameliorate disease symptoms in animal models.
In conclusion, Linvoseltamab Biosimilar, also known as Anti-TNFRSF17 mAb, is a research grade monoclonal antibody that specifically targets TNFRSF17, a key player in the pathogenesis of multiple myeloma and other B-cell malignancies. Its unique mechanism of action, including inhibition of TNFRSF17 signaling and induction of ADCC and CDC, makes it a promising candidate for the treatment of these diseases. Furthermore, its potential use in the treatment of autoimmune diseases adds to its versatility and potential impact in the medical field. Further clinical studies are needed to fully understand the efficacy and safety of this biosimilar, but early results are promising, making it a potential game-changer in the treatment of various diseases.
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