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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG4, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Spartalizumab Biosimilar - Anti-PDCD1, PD1, CD279 mAb - Research Grade |
|---|---|
| Source | CAS 1935694-88-4 |
| Species | Humanized |
| 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 | Spartalizumab,NPVPDR001,NVS240118,PDR001,PDCD1, PD1, CD279,anti-PDCD1, PD1, CD279 |
| Reference | PX-TA1483 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Spartalizumab Biosimilar, also known as Anti-PDCD1, PD1, CD279 mAb, is a novel monoclonal antibody that has shown promising results in the treatment of various cancers. This biosimilar is designed to target the programmed cell death protein 1 (PD-1) pathway, which plays a critical role in regulating the immune response. In this article, we will discuss the structure, activity, and potential applications of Spartalizumab Biosimilar in cancer research.
Spartalizumab Biosimilar is a fully humanized monoclonal antibody that is produced using recombinant DNA technology. It is composed of two identical heavy chains and two identical light chains, each containing a variable region and a constant region. The variable region of the antibody binds specifically to the PD-1 receptor, while the constant region determines the effector functions of the antibody.
The main mechanism of action of Spartalizumab Biosimilar is through its binding to the PD-1 receptor. PD-1 is a cell surface receptor that is expressed on activated T cells, B cells, and natural killer cells. Its ligands, PD-L1 and PD-L2, are expressed on various cancer cells and immune cells. The binding of PD-1 to its ligands leads to the inhibition of T cell activation and proliferation, thus allowing cancer cells to evade the immune response. Spartalizumab Biosimilar blocks this interaction, thereby enhancing the anti-tumor immune response.
Spartalizumab Biosimilar has shown promising results in preclinical and clinical studies for the treatment of various cancers. It has been investigated in both solid tumors and hematologic malignancies. Some of the potential applications of this biosimilar include:
1. Melanoma: Spartalizumab Biosimilar has been studied in combination with other anti- cancer therapies, such as chemotherapy and targeted therapy, in patients with advanced melanoma. It has shown significant clinical activity and has been well-tolerated in these patients.
2. Lung cancer: In a phase I study, Spartalizumab Biosimilar was evaluated in patients with advanced non-small cell lung cancer (NSCLC). The results showed that the biosimilar was well-tolerated and had promising anti-tumor activity in this patient population.
3. Lymphoma: Spartalizumab Biosimilar has also been investigated in patients with relapsed or refractory Hodgkin lymphoma and non-Hodgkin lymphoma. The results have shown that the biosimilar has significant clinical activity and is well-tolerated in these patients.
4. Solid tumors: In addition to the above-mentioned cancers, Spartalizumab Biosimilar has also been studied in other solid tumors, such as head and neck cancer, bladder cancer, and gastric cancer. The results have shown promising anti-tumor activity and a favorable safety profile.
Spartalizumab Biosimilar is a novel monoclonal antibody that targets the PD-1 pathway, which plays a critical role in regulating the immune response. Its structure, activity, and potential applications make it a promising candidate for the treatment of various cancers. Further studies are needed to fully understand the efficacy and safety of this biosimilar, but the current results are very promising. Spartalizumab Biosimilar has the potential to improve the outcomes of cancer patients and provide a new treatment option for those with limited options.
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