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View ProductsSize | 100ug, 1MG |
---|---|
Brand | ProteoGenix |
Isotype | IgG1-lambda2 |
Product type | Primary Antibodies |
Clonality | Monoclonal Antibody |
Expression system | XtenCHO |
Product name | Crebankitug Biosimilar - Anti-IL7R mAb - Research Grade |
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Source | CAS: 2893793-17-2 |
Origin species | Human |
Expression system | XtenCHO |
Purity | >95% by SDS-PAGE |
Buffer | 0.01M PBS, pH 7.4 |
Delivery condition | Blue ice (+4°C) |
Delivery lead time in business days | 3-5 days if in stock; 3-5 weeks if production needed |
Storage condition | 4°C for short term; -20°C for long term |
Brand | ProteoGenix |
Aliases /Synonyms | anti-IL7R, Interleukin-7 receptor subunit alpha, IL-7R-alpha, IL-7 receptor subunit alpha, CD127, CDw127, IL-7R subunit alpha, IL-7RA |
Reference | PX-TA2183-100 |
Note | For research use only. Not suitable for human use. |
Isotype | IgG1-lambda2 |
Clonality | Monoclonal Antibody |
Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade is a therapeutic antibody that specifically targets the IL7R protein. This biosimilar is a highly effective and safe treatment option for various autoimmune diseases, including rheumatoid arthritis, multiple sclerosis, and psoriasis. In this article, we will provide a detailed scientific description of the structure, activity, and application of Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade.
Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade is a monoclonal antibody (mAb) that is produced using recombinant DNA technology. It is a biosimilar of the therapeutic antibody Tocilizumab, which is currently used for the treatment of IL7R-related autoimmune diseases. The mAb has a molecular weight of approximately 148 kDa and is composed of two heavy chains and two light chains. The heavy chains are made up of approximately 450 amino acids, while the light chains consist of approximately 215 amino acids. The mAb has a Y-shaped structure, with two antigen-binding fragments (Fab) and one crystallizable fragment (Fc). The Fab regions are responsible for binding to the IL7R protein, while the Fc region is involved in immune effector functions.
The main activity of Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade is the inhibition of the IL7R protein. IL7R is a cell surface receptor that is present on various immune cells, including T cells and B cells. It plays a crucial role in the regulation of immune responses and is known to be overexpressed in autoimmune diseases. By binding to IL7R, Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade blocks its activity and prevents the activation of immune cells. This leads to a decrease in inflammation and tissue damage, resulting in the improvement of symptoms in patients with autoimmune diseases.
In addition to its inhibitory activity, Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade also has immune effector functions. These include antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC). ADCC involves the binding of the Fc region of the mAb to immune cells, such as natural killer cells, which then kill the target cells. CDC, on the other hand, involves the activation of the complement system, which leads to the lysis of target cells. These immune effector functions contribute to the overall therapeutic effect of Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade.
Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade is indicated for the treatment of various autoimmune diseases, including rheumatoid arthritis, multiple sclerosis, and psoriasis. It is administered via intravenous infusion and has been shown to be highly effective in reducing disease activity and improving symptoms in patients with these conditions. In addition, Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade has a good safety profile, with minimal side effects reported in clinical trials.
Furthermore, Crebankitug Biosimilar – Anti-IL7R mAb – Research Grade is also used in research studies to investigate the role of IL7R in different diseases and to develop new treatment strategies. Its high specificity and potency make it a valuable tool for studying the IL7R pathway and its potential as a therapeutic target.
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