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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Siplizumab Biosimilar - Anti-CD2, LFA-2 mAb - Research Grade |
|---|---|
| Source | CAS 288392-69-8 |
| Species | Humanized |
| Expression system | Mammalian cells |
| 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 | Siplizumab,MEDI-507,CD2, LFA-2,anti-CD2, LFA-2 |
| Reference | PX-TA1051 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Siplizumab Biosimilar, also known as Anti-CD2, LFA-2 mAb, is a monoclonal antibody (mAb) that targets the CD2 protein on the surface of T cells. It is a research grade antibody that has shown potential in various therapeutic applications. In this article, we will discuss the structure, activity, and potential applications of Siplizumab Biosimilar.
Siplizumab Biosimilar is a recombinant 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 region of the antibody is responsible for binding to the CD2 protein, while the constant region determines the antibody’s effector functions.
The variable region of Siplizumab Biosimilar is derived from a mouse monoclonal antibody, which has been genetically engineered to make it more similar to human antibodies. This process, known as humanization, reduces the risk of an immune response against the antibody when used in humans.
Siplizumab Biosimilar binds to the CD2 protein on the surface of T cells, which plays a critical role in T cell activation and communication with other immune cells. By binding to CD2, Siplizumab Biosimilar blocks the interaction between CD2 and its ligand, preventing T cell activation and proliferation.
In addition to blocking T cell activation, Siplizumab Biosimilar also has other mechanisms of action. It can induce antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), leading to the destruction of CD2-expressing cells. This makes Siplizumab Biosimilar a potential therapeutic agent for diseases involving abnormal T cell activation, such as autoimmune disorders and certain types of cancer.
Autoimmune Disorders Siplizumab Biosimilar has shown promising results in preclinical studies for the treatment of autoimmune disorders, such as rheumatoid arthritis and multiple sclerosis. By blocking T cell activation, it can reduce inflammation and tissue damage caused by overactive immune responses. Clinical trials are currently underway to evaluate the efficacy and safety of Siplizumab Biosimilar in these conditions.
CD2 is overexpressed on the surface of certain types of cancer cells, making it a potential therapeutic target. Siplizumab Biosimilar has shown promising results in preclinical studies for the treatment of leukemia and lymphoma. By inducing ADCC and CDC, it can selectively target and destroy cancer cells while sparing healthy cells. Clinical trials are ongoing to evaluate the efficacy and safety of Siplizumab Biosimilar in cancer treatment.
Organ rejection is a major concern in organ transplantation, and T cells play a crucial role in this process. Siplizumab Biosimilar has been studied as a potential immunosuppressive agent to prevent organ rejection by targeting T cell activation. Clinical trials have shown promising results in kidney transplantation, and further studies are ongoing to evaluate its potential in other types of organ transplantation.
IBD, including Crohn’s disease and ulcerative colitis, is characterized by chronic inflammation of the digestive tract. T cells play a critical role in the development and progression of IBD. Siplizumab Biosimilar has shown promising results in preclinical studies for the treatment of IBD by targeting T cell activation and reducing inflammation. Clinical trials are currently underway to evaluate its efficacy and safety in IBD patients.
Siplizumab Biosimilar - Anti-CD2, LFA-2 mAb, on SDS-PAGE under reducing and non-reducing condition. The gel was stained overnight with Coomassie Blue. The purity of the antibody is greater than 95%.
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