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| Size | 100ug, 1MG |
|---|---|
| Brand | ProteoGenix |
| Product type | Recombinant Proteins |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Belatacept Biosimilar - Anti-CD80, CD86 fusion protein - Research Grade |
|---|---|
| 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-CD80, B7-1, B7-2 CD86 |
| Reference | PX-TA2005 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | Fusion - [CTLA4 (cytotoxic T-lymphocyte-associated protein 4, CD152)]2 - IGHG1 Fc (Fragment constant) |
Belatacept Biosimilar is a novel fusion protein that has gained significant attention in the field of immunotherapy. This biosimilar is designed to target the CD80 and CD86 proteins, which are known to play a critical role in the activation of T cells. Belatacept Biosimilar has shown promising results in preclinical studies and is now being investigated for its potential therapeutic applications. In this article, we will provide a comprehensive scientific description of the structure, activity, and potential applications of Belatacept Biosimilar.
Belatacept Biosimilar is a fusion protein composed of the extracellular domain of human cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and the Fc portion of human IgG1. The CTLA-4 domain is responsible for binding to the CD80 and CD86 proteins, while the Fc portion provides stability and extended half-life to the fusion protein. The molecular weight of Belatacept Biosimilar is approximately 92 kDa.
Belatacept Biosimilar acts as an antagonist to the CD80 and CD86 proteins, which are co-stimulatory molecules expressed on antigen-presenting cells. These proteins are essential for the activation of T cells and play a critical role in the immune response. By binding to CD80 and CD86, Belatacept Biosimilar prevents their interaction with CD28, a co-stimulatory receptor on T cells. This results in the inhibition of T cell activation and proliferation, ultimately leading to immunosuppression.
Belatacept Biosimilar has shown high binding affinity and specificity towards CD80 and CD86, making it a potent antagonist of T cell activation. It is also known to induce a state of anergy in T cells, where they become unresponsive to further stimulation. This unique mechanism of action makes Belatacept Biosimilar a promising candidate for the treatment of various immune-mediated disorders.
Belatacept Biosimilar has shown promising results in preclinical studies for the treatment of various autoimmune and inflammatory disorders, including rheumatoid arthritis, psoriasis, and multiple sclerosis. It has also been investigated for its potential use in preventing transplant rejection in organ transplantation. In a phase III clinical trial, Belatacept Biosimilar showed superior efficacy and safety compared to the current standard of care, making it a potential alternative for immunosuppressive therapy in transplant patients.
Furthermore, Belatacept Biosimilar has also been studied for its potential use in the treatment of certain types of cancer. By inhibiting T cell activation, it can prevent the growth and spread of cancer cells, making it a promising therapeutic option for cancer immunotherapy.
In conclusion, Belatacept Biosimilar is a novel fusion protein that acts as an antagonist of the CD80 and CD86 proteins. Its unique mechanism of action makes it a potential therapeutic option for various immune-mediated disorders and cancer. With ongoing research and clinical trials, Belatacept Biosimilar has the potential to revolutionize the field of immunotherapy and improve the lives of patients suffering from these debilitating conditions.
Belatacept Biosimilar, fusion protein, CD80, CD86, T cells, immunotherapy, antagonist, co-stimulatory molecules, immune response, immunosuppression, autoimmune disorders, inflammatory disorders, organ transplantation, transplant rejection, cancer immunotherapy.
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