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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 | Miptenalimab Biosimilar - Anti-LAG3 mAb - Research Grade |
|---|---|
| Source | CAS 2249882-55-9 |
| Species | Humanized |
| Expression system | XtenCHO |
| 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 | Miptenalimab,BI754111,BI-754111, IMMUNOGLOBULIN G4 (230-PROLINE), ANTI-(HUMAN LYMPHOCYTE ACTIVATION GENE-3) (HUMAN MONOCLONAL BI754111 .GAMMA.4-CHAIN), DISULFIDE WITH HUMAN MONOCLONAL BI754111 .KAPPA.-CHAIN, DIMER,LAG3,anti-LAG3 |
| Reference | PX-TA1686 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4,Kappa |
| Clonality | Monoclonal Antibody |
Miptenalimab Biosimilar, also known as Anti-LAG3 mAb, is a research grade monoclonal antibody that has gained significant attention in the field of immunotherapy. This antibody is designed to target the Lymphocyte Activation Gene-3 (LAG-3) protein, which plays a crucial role in regulating the immune response. In this article, we will explore the structure, activity, and potential applications of Miptenalimab Biosimilar as a therapeutic agent.
Miptenalimab Biosimilar is a fully humanized monoclonal antibody, meaning it is derived from human cells and has a high affinity for its target protein. It consists of two identical heavy chains and two identical light chains, connected by disulfide bonds. The antibody has a molecular weight of approximately 150 kDa and belongs to the immunoglobulin G (IgG) class.
The variable region of Miptenalimab Biosimilar is responsible for binding to LAG-3, while the constant region mediates effector functions such as antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC). This unique structure allows Miptenalimab Biosimilar to specifically target LAG-3 expressing cells and initiate an immune response against them.
LAG-3 is a negative regulator of T cell activation and function. It is expressed on the surface of activated T cells, regulatory T cells, and natural killer (NK) cells. By binding to LAG-3, Miptenalimab Biosimilar blocks the interaction between LAG-3 and its ligands, such as MHC class II molecules, which are present on antigen-presenting cells.
This blockade leads to the activation and proliferation of T cells, as well as enhanced cytokine production. Additionally, Miptenalimab Biosimilar can also induce ADCC and CDC, resulting in the destruction of LAG-3 expressing cells. These mechanisms of action make Miptenalimab Biosimilar a promising immunotherapeutic agent for various diseases.
1.
Cancer immunotherapy: The overexpression of LAG-3 has been observed in various types of cancer, including melanoma, breast cancer, and lung cancer. By targeting LAG-3, Miptenalimab Biosimilar can enhance the anti-tumor immune response and potentially improve the efficacy of other cancer treatments.
2. Autoimmune diseases: LAG-3 is also involved in the development of autoimmune diseases, such as multiple sclerosis and rheumatoid arthritis. By inhibiting LAG-3, Miptenalimab Biosimilar can suppress the activity of autoreactive T cells and alleviate the symptoms of these diseases.
3.
Infectious diseases: LAG-3 is upregulated in chronic viral infections, such as HIV and hepatitis B, and is associated with T cell exhaustion. Miptenalimab Biosimilar can restore the function of exhausted T cells and enhance the immune response against these infections.
In summary, Miptenalimab Biosimilar is a research grade monoclonal antibody that specifically targets LAG-3 and has the potential to be used as a therapeutic agent in various diseases. Its unique structure and activity make it a promising immunotherapeutic option, and further research and clinical trials are needed to fully understand its potential in the treatment of diseases.
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