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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 |
| 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 monoclonal antibody (mAb), is a promising therapeutic agent that has shown significant potential in the treatment of various diseases. This biosimilar is a highly specific antibody that targets the TNFRSF17 protein, making it a valuable tool for researchers and clinicians alike. In this article, we will explore the structure, activity, and applications of Linvoseltamab Biosimilar in detail.
Linvoseltamab Biosimilar is a recombinant, humanized IgG1 monoclonal antibody that is produced in Chinese hamster ovary (CHO) cells. It is composed of two heavy chains and two light chains, each consisting of a variable and constant region. The variable region of the antibody is responsible for binding to the TNFRSF17 protein, while the constant region mediates effector functions such as antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC).
The primary activity of Linvoseltamab Biosimilar is the specific binding to the TNFRSF17 protein, which is overexpressed in various cancers and autoimmune diseases. This binding leads to the inhibition of TNFRSF17 signaling, which is involved in cell proliferation, survival, and differentiation. By blocking this signaling pathway, Linvoseltamab Biosimilar has the potential to inhibit tumor growth and reduce disease activity in autoimmune disorders.
Linvoseltamab Biosimilar has shown promising results in preclinical studies for the treatment of multiple myeloma, a type of blood cancer, and other hematologic malignancies. It has also shown potential in the treatment of autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. In addition, Linvoseltamab Biosimilar has been investigated as a potential therapy for solid tumors, including breast, lung, and ovarian cancers.
One of the major advantages of Linvoseltamab Biosimilar is its high specificity for the TNFRSF17 protein, which minimizes off-target effects and reduces the risk of adverse reactions. Additionally, as a biosimilar, it is highly similar to the reference product in terms of structure, function, and clinical efficacy. This allows for a more streamlined and cost-effective development process, making it more accessible to patients.
Linvoseltamab Biosimilar is currently in the early stages of clinical development, with several ongoing Phase 1 and Phase 2 clinical trials. These trials are evaluating the safety, efficacy, and pharmacokinetics of the biosimilar in various cancer and autoimmune disease indications. The results of these trials will provide valuable insights into the potential of Linvoseltamab Biosimilar as a therapeutic agent.
In conclusion, Linvoseltamab Biosimilar is a promising therapeutic agent that has shown significant potential in the treatment of various diseases. Its specific binding to the TNFRSF17 protein and its potential to inhibit tumor growth and reduce disease activity make it a valuable tool for researchers and clinicians. With ongoing clinical trials, we can expect to see more data on the safety and efficacy of this biosimilar, paving the way for its potential approval and use in the near future.
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