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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 | Atisnolerbart Biosimilar - Anti-BETVIA mAb - Research Grade |
|---|---|
| Species | Homo sapiens |
| Expression system | XtenCHO |
| Purity | >90% by SDS-PAGE. |
| Buffer | 0.01M PBS, pH 7.4. |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 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-BETVIA, Major pollen allergen Bet v 1-A, Allergen Bet v I-A, Bet v 1-A, BETVI |
| Reference | PX-TA2045 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Atisnolerbart Biosimilar – Anti-BETVIA mAb – Research Grade is a novel biosimilar antibody that targets the therapeutic protein BETVIA. This monoclonal antibody (mAb) has been specifically designed to mimic the structure and function of the original BETVIA-targeting antibody, making it a promising candidate for treating various diseases and disorders.
Atisnolerbart Biosimilar is a recombinant, fully humanized IgG1 monoclonal antibody. It is composed of two heavy chains and two light chains, each containing a variable region and a constant region. The variable regions are responsible for binding to the therapeutic target, BETVIA, while the constant regions provide stability and effector functions.
Atisnolerbart Biosimilar exerts its activity by binding to BETVIA with high specificity and affinity. This binding prevents BETVIA from interacting with its cellular receptors, thereby inhibiting its biological activity. As a result, the downstream signaling pathways and cellular processes regulated by BETVIA are also inhibited.
Atisnolerbart Biosimilar has potential applications in various therapeutic areas. Its primary use is in the treatment of diseases and disorders that are associated with overexpression or dysregulation of BETVIA. These include inflammatory conditions, autoimmune diseases, and certain types of cancer.
BETVIA is known to play a crucial role in the development and progression of inflammatory conditions such as rheumatoid arthritis, psoriasis, and inflammatory bowel disease. By inhibiting BETVIA, Atisnolerbart Biosimilar can reduce inflammation and alleviate symptoms associated with these conditions.
Autoimmune diseases, such as multiple sclerosis and lupus, are characterized by an overactive immune response against the body’s own tissues. BETVIA has been implicated in the pathogenesis of these diseases, and Atisnolerbart Biosimilar can potentially modulate the immune response by targeting BETVIA.
BETVIA is also involved in the growth and survival of certain types of cancer cells. By blocking BETVIA, Atisnolerbart Biosimilar can inhibit the proliferation and survival of these cancer cells, making it a potential therapeutic option for cancer treatment.
Atisnolerbart Biosimilar is currently available in a research-grade form, which is intended for use in preclinical and clinical research studies. This grade of the antibody is produced using high-quality, state-of-the-art technology, ensuring consistency and purity for reliable and reproducible results.
Compared to the original BETVIA-targeting antibody, Atisnolerbart Biosimilar offers several advantages. As a biosimilar, it has a similar structure and function to the original antibody, making it highly specific and effective. Additionally, being a fully humanized antibody, it has a lower risk of immunogenicity and can be used in a wider range of patients.
Atisnolerbart Biosimilar – Anti-BETVIA mAb – Research Grade is a promising antibody with potential applications in various therapeutic areas. Its specific structure and activity make it a valuable tool for research studies, and its potential to target BETVIA in diseases and disorders makes it a promising candidate for future clinical use. Its availability in a research-grade form allows for further exploration of its therapeutic potential and paves the way for its development as a novel treatment option.
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