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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 | Stapokibart Biosimilar - Anti-IL-4RA mAb - Research Grade |
|---|---|
| Source | CAS: 2734715-10-5 |
| Species | Human |
| Buffer | 0.01M PBS, pH 7.4 |
| 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 | anti-IL-4RA, IL-4-binding protein, IL-4 receptor subunit alpha, Soluble IL-4R-alpha, IL4-BP, IL4R, IL-4R subunit alpha, IL-4R-alpha, CD124, Interleukin-4 receptor subunit alpha, IL4RA, Soluble IL-4 receptor subunit alpha, sIL4Ralpha/prot |
| Reference | PX-TA1966 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Stapokibart Biosimilar – Anti-IL-4RA mAb is a novel antibody-based therapeutic agent that has been developed to target the interleukin-4 receptor alpha (IL-4RA), a key player in the immune response and inflammation. This biosimilar is a highly specific and potent inhibitor of IL-4RA, and has shown promising results in pre-clinical studies. In this article, we will provide a detailed description of the structure, activity, and potential applications of this biosimilar.
Stapokibart Biosimilar – Anti-IL-4RA mAb is a monoclonal antibody (mAb) that is produced using recombinant DNA technology. It is a fully humanized mAb, meaning that it is derived from human antibody sequences and has a high degree of similarity to natural human antibodies. This makes it less likely to cause an immune response in patients, reducing the risk of adverse reactions.
The biosimilar consists of two identical heavy chains and two identical light chains, connected by disulfide bonds. The heavy chains are composed of four constant regions (Fc) and one variable region (VH), while the light chains have two constant regions (CL) and one variable region (VL). The variable regions are responsible for binding to the target IL-4RA, while the constant regions determine the effector functions of the antibody.
Stapokibart Biosimilar – Anti-IL-4RA mAb exerts its activity by binding to the IL-4RA on the surface of immune cells, such as T cells, B cells, and mast cells. This binding prevents the binding of the natural ligands of IL-4RA, interleukin-4 (IL-4) and interleukin-13 (IL-13), and thus inhibits the downstream signaling pathways that lead to inflammation and immune response.
IL-4RA is a crucial receptor in the immune system, and its dysregulation has been linked to various inflammatory diseases, such as asthma, atopic dermatitis, and rheumatoid arthritis. By inhibiting IL-4RA, Stapokibart Biosimilar – Anti-IL-4RA mAb has the potential to treat these diseases by reducing inflammation and modulating the immune response.
Stapokibart Biosimilar – Anti-IL-4RA mAb is currently being investigated for its potential use in the treatment of various inflammatory diseases. Pre-clinical studies have shown promising results in animal models of asthma and atopic dermatitis, where the biosimilar was able to reduce airway inflammation and improve skin lesions, respectively.
In addition to these indications, Stapokibart Biosimilar – Anti-IL-4RA mAb may also have potential applications in other diseases where IL-4RA plays a role. These include allergic rhinitis, chronic obstructive pulmonary disease (COPD), and inflammatory bowel disease (IBD). Clinical trials are currently ongoing to evaluate the safety and efficacy of this biosimilar in these indications.
In summary, Stapokibart Biosimilar – Anti-IL-4RA mAb is a novel antibody-based therapeutic agent that targets the IL-4RA, a key player in the immune response and inflammation. Its unique structure and mechanism of action make it a promising candidate for the treatment of various inflammatory diseases. Further clinical studies will determine its safety and efficacy and may lead to its approval for clinical use.
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