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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 | Atidortoxumab Biosimilar - Anti-alpha toxin mAb - Research Grade |
|---|---|
| Source | CAS 1939108-95-8 |
| Species | Homo sapiens |
| Expression system | Mammalian cells |
| 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 | Staphylococcus aureus,ASN-1,ASN-100 (combination of atidortoxumab and berlimatoxumab),alpha toxin,anti-alpha toxin |
| Reference | PX-TA1485 |
| Note | For research use only. Not suitable for human use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Atidortoxumab Biosimilar: A Promising Anti-Alpha Toxin Monoclonal Antibody for Therapeutic Applications Atidortoxumab Biosimilar, also known as anti-alpha toxin mAb, is a research grade monoclonal antibody that has shown promising potential as a therapeutic agent for a variety of diseases. This biosimilar is a highly specific antibody that targets the alpha toxin, a virulence factor produced by various bacterial pathogens.
Atidortoxumab Biosimilar is a recombinant humanized monoclonal antibody that is structurally similar to the original Atidortoxumab. It consists of two identical heavy chains and two identical light chains, each with a molecular weight of approximately 150 kDa. The heavy and light chains are connected by disulfide bonds and form a Y-shaped structure, with the antigen-binding sites located at the tips of the arms.
The variable regions of the antibody, also known as the antigen-binding regions, are responsible for the specificity of Atidortoxumab Biosimilar towards the alpha toxin. These regions are highly diverse and are generated through genetic recombination during the development of B-cells. The constant regions of the antibody, on the other hand, are responsible for the effector functions of the antibody, such as binding to immune cells and activating the complement system.
Atidortoxumab Biosimilar exerts its therapeutic effects by binding to the alpha toxin produced by bacterial pathogens. This binding prevents the toxin from interacting with its target cells and inhibits its cytotoxic activity. Additionally, the binding of the antibody to the toxin also triggers the immune system to recognize and eliminate the toxin, further enhancing its efficacy.
Moreover, Atidortoxumab Biosimilar can also activate the complement system, a part of the immune system that helps in the clearance of pathogens. This activation leads to the formation of membrane attack complexes that can directly lyse bacterial cells, providing an additional mechanism of action for the antibody.
Atidortoxumab Biosimilar has been studied for its therapeutic potential in various diseases caused by bacterial pathogens that produce the alpha toxin. Some of the notable applications of this antibody include:
1. Treatment of Staphylococcus aureus infections Staphylococcus aureus is a common bacterial pathogen that produces the alpha toxin, which is responsible for the development of severe skin and soft tissue infections. Atidortoxumab Biosimilar has shown promising results in preclinical studies as a potential treatment for these infections. It has been found to effectively neutralize the alpha toxin and inhibit its cytotoxic effects, leading to improved outcomes in animal models.
2. Prevention of Clostridium perfringens infections Clostridium perfringens is a bacterium that produces the alpha toxin, which is responsible for the development of gas gangrene and food poisoning. Atidortoxumab Biosimilar has been shown to effectively neutralize the alpha toxin and prevent its cytotoxic effects, making it a potential preventive measure against these infections.
3. Treatment of necrotizing fasciitis Necrotizing fasciitis is a severe and potentially life-threatening infection caused by bacterial pathogens, including Streptococcus pyogenes, which produce the alpha toxin. Atidortoxumab Biosimilar has shown promising results in preclinical studies as a potential treatment for this infection. It has been found to effectively neutralize the alpha toxin and reduce tissue damage, leading to improved outcomes in animal models.
4. Management of sepsis Sepsis is a life-threatening condition caused by an overwhelming immune response to an infection. Bacterial
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