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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Nofetumomab Biosimilar - Anti-CD20/MS4A1 mAb - Research Grade |
|---|---|
| Source | CAS 165942-79-0 |
| Species | Humanized |
| Purity | >85% |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Nofetumomab ,Technetium (99mTc)Nofetumomab Merpentan,CD20/MS4A1 ,anti-CD20/MS4A2 |
| Reference | PX-TA1093 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Nofetumomab Biosimilar, also known as Anti-CD20/MS4A1 mAb, is a monoclonal antibody (mAb) that specifically targets CD20, a protein found on the surface of B cells. This biosimilar is a highly effective therapeutic agent in the treatment of various B cell-related diseases, including non-Hodgkin’s lymphoma, chronic lymphocytic leukemia, and rheumatoid arthritis.
Nofetumomab Biosimilar is a recombinant humanized IgG1 monoclonal antibody, meaning it is produced by genetically engineering human genes into a non-human host, in this case, Chinese hamster ovary (CHO) cells. The antibody has a molecular weight of approximately 150 kDa and consists of two heavy chains and two light chains, connected by disulfide bonds.
The heavy chains are composed of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chains contain two constant domains (CL and CL1) and one variable domain (VL). The variable domains are responsible for binding to the target protein, CD20, while the constant domains provide stability and effector functions.
The binding site of Nofetumomab Biosimilar is located on the Fab region, which is the fragment antigen-binding region of the antibody. This region is highly specific and complementary to the CD20 protein, allowing for a strong and selective binding interaction.
Nofetumomab Biosimilar exerts its therapeutic effects by binding to the CD20 protein on the surface of B cells. This binding triggers a cascade of events that leads to the destruction of the B cells, either by direct cell death or through the activation of the immune system.
One of the main mechanisms of action of Nofetumomab Biosimilar is antibody-dependent cell-mediated cytotoxicity (ADCC). This occurs when the antibody binds to the CD20 protein, and the Fc region of the antibody interacts with immune cells, such as natural killer (NK) cells and macrophages. These immune cells then release cytotoxic substances, such as perforin and granzymes, which induce cell death in the B cells.
Another mechanism of action is complement-dependent cytotoxicity (CDC). In this process, the binding of Nofetumomab Biosimilar to CD20 triggers the activation of the complement system, leading to the formation of a membrane attack complex that causes cell lysis.
Nofetumomab Biosimilar is primarily used as a therapeutic agent in the treatment of B cell-related diseases. It has been approved for the treatment of non-Hodgkin’s lymphoma and chronic lymphocytic leukemia, and is also being investigated for its potential in treating other B cell-related disorders, such as multiple sclerosis and lupus nephritis.
In addition to its therapeutic applications, Nofetumomab Biosimilar is also used in research settings as a tool for studying the role of CD20 in various diseases and for developing new treatments targeting this protein.
Nofetumomab Biosimilar is a potent anti-CD20 antibody with a well-defined structure and mechanism of action. Its ability to selectively bind to CD20 and induce the destruction of B cells makes it a highly effective therapeutic agent for various B cell-related diseases. With ongoing research and development, this biosimilar has the potential to revolutionize the treatment of these diseases and improve the lives of patients worldwide.
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