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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG4-lambda |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Teclistamab Biosimilar - Anti-BCMA-CD3 mAb - Research Grade |
|---|---|
| Source | CAS 2119595-80-9 |
| Species | Chimeric, Homo sapiens |
| 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 | Teclistamab ,JNJ-64007957,MS4A1,anti-MS4A1 |
| Reference | PX-TA1550 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-lambda |
| Clonality | Monoclonal Antibody |
Teclistamab Biosimilar, also known as Anti-BCMA-CD3 mAb, is a novel antibody that has been developed for the treatment of multiple myeloma, a type of cancer that affects the plasma cells in the bone marrow. This biosimilar is a research grade version of the original Teclistamab antibody and has been designed to specifically target the B-cell maturation antigen (BCMA) on the surface of cancer cells. In this article, we will discuss the structure, activity, and potential applications of Teclistamab Biosimilar in the field of cancer research.
Teclistamab Biosimilar is a monoclonal antibody, which means it is a laboratory-produced protein that is designed to mimic the natural antibodies produced by our immune system. It is composed of two different types of proteins – the constant region and the variable region. The constant region is responsible for the effector functions of the antibody, while the variable region is responsible for binding to the target antigen, in this case, BCMA.
The antibody is composed of two heavy chains and two light chains, which are held together by disulfide bonds. The heavy chains contain the constant regions CH1, CH2, CH3, and the variable region VH, while the light chains contain the constant regions CL and the variable region VL. The variable regions of the heavy and light chains come together to form the antigen-binding site, which is responsible for the specificity of the antibody towards its target.
Teclistamab Biosimilar is a bispecific antibody, meaning it has two different binding sites – one for BCMA and one for CD3. BCMA is a protein that is overexpressed on the surface of multiple myeloma cells, making it an ideal therapeutic target. CD3, on the other hand, is a protein found on the surface of T cells, which are a type of immune cells responsible for recognizing and destroying cancer cells.
When Teclistamab Biosimilar binds to both BCMA and CD3, it brings the cancer cells and T cells into close proximity, leading to the activation and proliferation of the T cells. This results in the destruction of the cancer cells, making Teclistamab Biosimilar an effective anti- cancer therapy.
Teclistamab Biosimilar has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of multiple myeloma. It has the potential to become a targeted therapy for patients with relapsed or refractory multiple myeloma, as well as for those who have become resistant to other treatments.
In addition to its potential as a monotherapy, Teclistamab Biosimilar also has the potential to be used in combination with other anti- cancer therapies, such as chemotherapy and other targeted therapies. This could potentially enhance the efficacy of these treatments and improve patient outcomes.
In conclusion, Teclistamab Biosimilar is a novel antibody with a unique structure and mechanism of action. Its ability to target both BCMA and CD3 makes it a promising therapeutic option for patients with multiple myeloma. As research on this biosimilar continues, it has the potential to become a valuable addition to the arsenal of treatments available for this type of cancer.
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