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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 | Nurulimab Biosimilar - Anti-CTLA4 mAb - Research Grade |
|---|---|
| Species | Homo sapiens |
| 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 | Nurulimab ,BCD-145,CTLA4,anti-CTLA4 |
| Reference | PX-TA1597 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Nurulimab Biosimilar, also known as anti-CTLA4 monoclonal antibody (mAb), is a novel therapeutic agent that has shown great promise in the treatment of various diseases. This biosimilar is a replica of the original Nurulimab, which is a humanized IgG1 mAb targeting the cytotoxic T-lymphocyte-associated protein 4 (CTLA4). In this article, we will explore the structure, activity, and potential applications of Nurulimab Biosimilar as a therapeutic antibody.
Nurulimab Biosimilar is a recombinant protein produced through genetic engineering techniques. It is composed of two identical heavy chains and two identical light chains, each with a molecular weight of approximately 150 kDa. The heavy and light chains are connected by disulfide bonds, forming a Y-shaped structure. The variable regions of the heavy and light chains are responsible for binding to the target antigen, CTLA4.
The amino acid sequence of Nurulimab Biosimilar is highly similar to that of the original Nurulimab, making it a highly specific and potent therapeutic agent. Its structure is designed to mimic the natural human IgG1 antibody, allowing it to interact with the immune system without causing any adverse effects.
Nurulimab Biosimilar binds to CTLA4, a protein found on the surface of T-cells, and acts as an immune checkpoint inhibitor. CTLA4 is a negative regulator of T-cell activation and plays a crucial role in maintaining immune homeostasis. By blocking CTLA4, Nurulimab Biosimilar enhances the activation of T-cells, leading to an increased immune response against cancer cells and other diseases.
Studies have shown that Nurulimab Biosimilar has a high binding affinity for CTLA4, with an equilibrium dissociation constant (Kd) in the nanomolar range. This strong binding allows for efficient inhibition of CTLA4 and subsequent T-cell activation.
As an anti-CTLA4 mAb, Nurulimab Biosimilar has shown promising results in the treatment of various diseases, especially cancer. It has been extensively studied in clinical trials for the treatment of melanoma, non-small cell lung cancer, and renal cell carcinoma. In these trials, Nurulimab Biosimilar has demonstrated significant antitumor activity, leading to its approval for use in these cancers.
In addition to cancer, Nurulimab Biosimilar has also shown potential in the treatment of autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis. By inhibiting CTLA4, this biosimilar can modulate the immune response and reduce inflammation, providing relief to patients with these conditions.
Furthermore, Nurulimab Biosimilar has also been investigated as a potential therapy for organ transplant rejection. By preventing the inactivation of T-cells, it can help prevent the rejection of transplanted organs and improve patient outcomes.
Nurulimab Biosimilar is a highly promising therapeutic agent that has shown great potential in the treatment of various diseases. Its specific structure and strong binding to CTLA4 make it a potent anti-CTLA4 mAb with minimal side effects. With its approval for use in cancer and ongoing research in other diseases, Nurulimab Biosimilar is set to revolutionize the field of immunotherapy and provide new treatment options for patients in need.
Keywords: Nurulimab Biosimilar, anti-CTLA4 mAb, therapeutic target, antibody, immunotherapy, cancer, autoimmune diseases, organ transplant rejection.
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