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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 | Urtoxazumab Biosimilar - Anti-Stx-2, SLT-II mAb - Research Grade |
|---|---|
| Source | CAS 502496-16-4 |
| Species | Humanized |
| Expression system | Mammalian cells |
| 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 | Urtoxazumab,HuVTm1.1,TMA-15,Stx-2, SLT-II,anti-Stx-2, SLT-II |
| Reference | PX-TA1190 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Urtoxazumab Biosimilar – Anti-Stx-2, SLT-II mAb – Research Grade is a monoclonal antibody that has been developed as a biosimilar to Urtoxazumab, a therapeutic antibody used in the treatment of Shiga toxin-producing E. coli (STEC) infections. This biosimilar has been designed to specifically target Stx-2, one of the main toxins produced by STEC, making it a promising therapeutic option for patients with STEC infections.
Urtoxazumab Biosimilar is a monoclonal antibody, meaning it is produced by a single type of immune cell and is therefore highly specific in its target binding. The antibody is composed of two identical heavy chains and two identical light chains, connected by disulfide bonds. The heavy chains contain a variable region, responsible for binding to the target, and a constant region, which determines the antibody’s class and effector functions. The light chains also have a variable and constant region, but are smaller in size compared to the heavy chains.
The main activity of Urtoxazumab Biosimilar is to bind to Stx-2, preventing it from binding to its target receptors on host cells. Stx-2 is a potent toxin produced by STEC, which can cause severe gastrointestinal and neurological symptoms in infected individuals. By binding to Stx-2, Urtoxazumab Biosimilar prevents the toxin from entering host cells and causing damage. This neutralizing activity of the biosimilar can help in reducing the severity of symptoms and improving the outcome of STEC infections.
In addition to its neutralizing activity, Urtoxazumab Biosimilar also has effector functions that can help in clearing Stx-2 from the body. These include antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC). In ADCC, the antibody binds to Stx-2 and recruits immune cells, such as natural killer cells, to destroy the target. In CDC, the antibody binds to Stx-2 and activates the complement system, leading to the lysis of the target.
Urtoxazumab Biosimilar has shown promising results in preclinical studies as a potential treatment for STEC infections. Its specificity and neutralizing activity make it a promising alternative to Urtoxazumab, which has shown limited efficacy in clinical trials. The biosimilar can also be used as a prophylactic treatment for individuals at high risk of STEC infections, such as those with compromised immune systems.
In addition to its therapeutic potential, Urtoxazumab Biosimilar can also be a valuable tool in research and diagnostics. Its specificity for Stx-2 makes it a useful reagent for detecting and quantifying the toxin in clinical samples. It can also be used in research studies to better understand the mechanisms of STEC infections and develop new treatments.
In summary, Urtoxazumab Biosimilar – Anti-Stx-2, SLT-II mAb – Research Grade is a monoclonal antibody that specifically targets Stx-2, a toxin produced by STEC. Its structure, activity, and applications make it a promising therapeutic option for STEC infections, as well as a valuable tool in research and diagnostics. Further clinical trials are needed to evaluate the efficacy and safety of this biosimilar, but it holds great potential in improving the treatment and prevention of STEC infections.
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