No services found
No Products found
100ug, 1MG
ProteoGenix
IgG1, kappa
Primary Antibodies
Monoclonal Antibody
XtenCHO
Tazlestobart Biosimilar, also known as Anti-CD152 mAb, is a therapeutic antibody that has been developed for the treatment of various diseases. It is a biosimilar version of the existing therapeutic antibody, which has shown promising results in clinical trials. In this article, we will discuss the structure, activity, and application of Tazlestobart Biosimilar in detail.
Tazlestobart Biosimilar is a monoclonal antibody that specifically targets CD152, also known as cytotoxic T-lymphocyte-associated protein 4 (CTLA-4). It is a fully humanized antibody, meaning it is derived from human cells, making it less likely to cause an immune response in patients. The antibody consists of two heavy chains and two light chains, connected by disulfide bonds. The heavy chains are composed of constant and variable regions, while the light chains only have variable regions. The variable regions are responsible for binding to the CD152 receptor, while the constant regions determine the antibody’s effector function.
Tazlestobart Biosimilar works by binding to the CD152 receptor on the surface of T cells. This receptor is a negative regulator of T cell activation, meaning it inhibits the activation of T cells. By binding to CD152, Tazlestobart Biosimilar prevents the interaction of CD152 with its ligands, CD80 and CD86, which are present on antigen-presenting cells. This results in the activation of T cells, leading to an enhanced immune response against cancer cells or other disease-causing agents. Additionally, Tazlestobart Biosimilar can also induce antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), which further contribute to its therapeutic activity.
Tazlestobart Biosimilar has shown promising results in clinical trials for the treatment of various diseases, including cancer and autoimmune disorders. In cancer, Tazlestobart Biosimilar has been studied as a monotherapy and in combination with other therapies, such as chemotherapy and other immunotherapies. It has shown efficacy in various types of cancer, including melanoma, non-small cell lung cancer, and renal cell carcinoma. In autoimmune disorders, Tazlestobart Biosimilar has been studied for the treatment of rheumatoid arthritis, psoriasis, and multiple sclerosis. Its ability to modulate the immune response makes it a potential treatment option for these diseases.
CD152, the therapeutic target of Tazlestobart Biosimilar, is a protein that is primarily expressed on the surface of T cells. It is a negative regulator of T cell activation, meaning it inhibits the activation of T cells. This is important in maintaining immune homeostasis and preventing autoimmune responses. However, in diseases such as cancer, CD152 can be upregulated, leading to a suppression of the immune response against cancer cells. By targeting CD152, Tazlestobart Biosimilar can enhance the immune response against cancer cells and potentially improve patient outcomes.
In summary, Tazlestobart Biosimilar is a therapeutic antibody that specifically targets CD152. It has a unique structure and mechanism of action, which allows it to modulate the immune response and potentially treat a wide range of diseases. Its promising results in clinical trials make it a potential treatment option for cancer and autoimmune disorders. Further research and development of Tazlestobart Biosimilar may lead to its approval and availability for patients in need.
Reviews
There are no reviews yet.
Your email address will not be published. Required fields are marked *
In which application did you use the antibody? * WB ELISA Sandwich ELISA IF IHC IP FC other
Did it work in your application? * Yes No
Your review *
Name *
Email *
Save my name, email, and website in this browser for the next time I comment.
Related products
Got a question or need a quote? Message us and we’ll get back to you 48 hours or less.
First name
Last name
Email address
Lab / Company
Phone number
send
Your cart is currently empty.