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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 | Amatuximab Biosimilar - Anti-MSLN mAb - Research Grade |
|---|---|
| Source | CAS 931402-35-6 |
| Species | Chimeric |
| Expression system | Mammalian cells |
| Molecular weight | 144kDa |
| Purity | >85% |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery lead time in business days | 3-5 days if in stock; 3-5 weeks if production needed |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Amatuximab,MORAb-009,MSLN,anti-MSLN |
| Reference | PX-TA1049 |
| Note | For research use only. Not suitable for human use. |
| Isotype | IgG1-kappa |
Amatuximab Biosimilar, also known as Anti-MSLN mAb, is a monoclonal antibody (mAb) that has shown promising results in the treatment of various cancers. This biosimilar version of the original Amatuximab has been developed to provide a more affordable and accessible option for patients. In this article, we will delve into the structure, activity, and potential applications of Amatuximab Biosimilar.
Amatuximab Biosimilar is a recombinant humanized IgG1 monoclonal antibody that has been designed to target the mesothelin (MSLN) protein. The antibody has a molecular weight of approximately 150 kDa and is composed of two heavy chains and two light chains. The heavy chains consist of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chains consist of two constant domains (CL and CL2) and one variable domain (VL).
The variable domains of Amatuximab Biosimilar are responsible for binding to MSLN, while the constant domains are responsible for mediating effector functions such as antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC). The antibody has been engineered to have a longer half-life and improved binding affinity compared to the original Amatuximab, making it a more potent therapeutic agent.
Amatuximab Biosimilar works by targeting the MSLN protein, which is overexpressed in various cancers, including mesothelioma, ovarian cancer, and pancreatic cancer. MSLN is a cell surface glycoprotein that plays a crucial role in cell adhesion, proliferation, and invasion. By binding to MSLN, Amatuximab Biosimilar inhibits these processes and induces cell death through various mechanisms.
One of the main mechanisms of action of Amatuximab Biosimilar is ADCC, where the antibody binds to MSLN-expressing cancer cells and recruits immune cells, such as natural killer (NK) cells, to kill the target cells. The antibody also activates the complement system, leading to the formation of membrane attack complexes that can directly kill cancer cells.
Amatuximab Biosimilar has shown promising results in preclinical and clinical studies for the treatment of various cancers. In particular, it has shown efficacy in mesothelioma, a rare and aggressive cancer that is often resistant to chemotherapy. The antibody has also shown potential in other MSLN-expressing cancers, such as ovarian and pancreatic cancer.
Currently, Amatuximab Biosimilar is being evaluated in phase II clinical trials for the treatment of mesothelioma and ovarian cancer. The results from these trials have shown promising efficacy and safety profiles, with some patients experiencing partial or complete remission. If these trials are successful, Amatuximab Biosimilar could potentially become a valuable treatment option for patients with these types of cancers.
In conclusion, Amatuximab Biosimilar is a promising anti-MSLN mAb that has been developed as a biosimilar version of the original Amatuximab. Its unique structure and activity make it a potent therapeutic agent for various MSLN-expressing cancers. With ongoing clinical trials, Amatuximab Biosimilar has the potential to become a valuable treatment option for patients in need.
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