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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG2-lambda |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Brazikumab Biosimilar - Anti-IL23A mAb - Research Grade |
|---|---|
| Source | CAS 1610353-18-8 |
| Species | Homo sapiens |
| 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 | Brazikumab,AMG-139,MEDI2070,IL23A,anti-IL23A |
| Reference | PX-TA1449 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG2-lambda |
| Clonality | Monoclonal Antibody |
Brazikumab Biosimilar, also known as Anti-IL23A mAb, is a research grade monoclonal antibody that targets the interleukin-23A (IL-23A) protein. IL-23A is a cytokine that plays a key role in the development and maintenance of chronic inflammatory diseases, making it a promising therapeutic target for various conditions. In this article, we will explore the structure, activity, and potential applications of Brazikumab Biosimilar.
Brazikumab Biosimilar is a recombinant humanized monoclonal antibody that is designed to mimic the structure and function of the naturally occurring antibody. It is composed of two identical heavy chains and two identical light chains, each containing a variable region and a constant region. The variable regions of the antibody are responsible for binding to the IL-23A protein, while the constant regions provide stability and effector functions.
Brazikumab Biosimilar works by specifically targeting and binding to the IL-23A protein, thereby inhibiting its activity. IL-23A is a pro-inflammatory cytokine that is produced by various immune cells, such as dendritic cells and macrophages. It plays a crucial role in the differentiation and activation of Th17 cells, which are a type of T-helper cell involved in the pathogenesis of many autoimmune and inflammatory diseases.
By binding to IL-23A, Brazikumab Biosimilar prevents its interaction with its receptor and blocks the downstream signaling pathways that lead to the production of pro-inflammatory cytokines. This results in a reduction of Th17 cell activity and a decrease in inflammation, making Brazikumab Biosimilar a promising therapeutic option for various chronic inflammatory diseases.
Brazikumab Biosimilar has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of various conditions, including psoriasis, psoriatic arthritis, Crohn’s disease, and ulcerative colitis. These are all chronic inflammatory diseases that are characterized by an overactive immune response and are associated with elevated levels of IL-23A.
The potential applications of Brazikumab Biosimilar extend beyond these conditions, as IL-23A has been implicated in the pathogenesis of other autoimmune and inflammatory diseases, such as rheumatoid arthritis, ankylosing spondylitis, and multiple sclerosis. Therefore, Brazikumab Biosimilar has the potential to be a versatile treatment option for a wide range of chronic inflammatory conditions.
Brazikumab Biosimilar, also known as Anti-IL23A mAb, is a research grade monoclonal antibody that specifically targets and inhibits the activity of the pro-inflammatory cytokine IL-23A. Its unique structure and mechanism of action make it a promising therapeutic option for various chronic inflammatory diseases. With ongoing clinical trials, Brazikumab Biosimilar has the potential to provide a much-needed treatment option for patients suffering from these conditions.
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