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| Size | 100ug, 1MG |
|---|---|
| Brand | ProteoGenix |
| Product type | Recombinant Proteins |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Alefacept Biosimilar - Anti-CD2 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-Erythrocyte receptor, SRBC, T-cell surface antigen CD2, Rosette receptor, CD2, LFA-3 receptor, T-cell surface antigen T11/Leu-5, LFA-2 |
| Reference | PX-TA2000 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | Fusion - [CD58 (LFA3, lymphocyte function associated antigen 3)]2 - IGHG1 Fc (Fragment constant) |
Alefacept Biosimilar, also known as Anti-CD2 fusion protein, is a research grade antibody that has been developed as a therapeutic agent for various immune-mediated diseases. This biosimilar is a recombinant fusion protein that targets the CD2 antigen on T cells, and has shown promising results in clinical trials for the treatment of psoriasis and other autoimmune disorders. In this article, we will delve into the structure, activity, and potential applications of Alefacept Biosimilar.
Alefacept Biosimilar is a fusion protein composed of the extracellular domain of human CD2 and the Fc portion of human IgG1. The CD2 domain is responsible for binding to the CD2 receptor on T cells, while the Fc portion provides stability and prolongs the half-life of the protein in the body. The structure of Alefacept Biosimilar is similar to the original drug, Alefacept, which was approved by the FDA in 2003 for the treatment of psoriasis.
The primary target of Alefacept Biosimilar is the CD2 antigen, which is expressed on the surface of T cells. CD2 is involved in T cell activation and proliferation, and its binding with Alefacept Biosimilar inhibits the interaction between T cells and antigen-presenting cells. This leads to a decrease in the production of pro-inflammatory cytokines and a reduction in T cell-mediated immune responses. In addition, Alefacept Biosimilar also promotes the death of activated T cells, further reducing their numbers in the body. This dual mechanism of action makes Alefacept Biosimilar an effective therapeutic agent for immune-mediated diseases.
The most well-studied application of Alefacept Biosimilar is in the treatment of psoriasis, a chronic inflammatory skin disease. Clinical trials have shown that Alefacept Biosimilar can significantly improve symptoms of psoriasis, such as skin plaques, scaling, and itching. It is also being investigated as a potential treatment for other autoimmune disorders, including rheumatoid arthritis, multiple sclerosis, and type 1 diabetes. In these conditions, Alefacept Biosimilar may help to reduce the overactive immune response that leads to tissue damage and inflammation.
It is important to note that Alefacept Biosimilar is currently only available in research grade, meaning it is intended for use in laboratory studies and clinical trials. This is different from therapeutic grade, which is the grade of a drug that has been approved for use in patients. While Alefacept Biosimilar has shown promising results in clinical trials, it has not yet been approved for therapeutic use. However, the research grade version of the drug is still crucial for further studies and development of the therapeutic grade version.
In summary, Alefacept Biosimilar is a research grade antibody that targets the CD2 antigen on T cells. Its structure, composed of the CD2 domain and Fc portion, allows for effective binding and inhibition of T cell activation and proliferation. This makes it a promising therapeutic agent for immune-mediated diseases, particularly psoriasis. Further research and clinical trials are needed to fully understand the potential applications of Alefacept Biosimilar and to develop a therapeutic grade version for use in patients.
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