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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Vulinacimab Biosimilar - Anti-VEGFR2 mAb - Research Grade |
|---|---|
| Source | CAS 2250342-36-8 |
| 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 week if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Vulinacimab,ANTI-VEGFR2 MONOCLONAL ANTIBODY HLX06, IMMUNOGLOBULIN G1, ANTI-(HUMAN VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 2)(HUMAN MONOCLONAL HLX06 .GAMMA.1-CHAIN), DISULFIDE WITH HUMAN MONOCLONAL HLX06 .KAPPA.-CHAIN), DIMER, ANTI P35968 (VGFR2_HUMAN),VEGFR2,anti-VEGFR2 |
| Reference | PX-TA1740 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1,Kappa |
| Clonality | Monoclonal Antibody |
Vulinacimab Biosimilar, also known as Anti-VEGFR2 mAb, is a monoclonal antibody that targets the vascular endothelial growth factor receptor 2 (VEGFR2). It is a research grade antibody that has shown promising results in pre-clinical studies and is currently being evaluated for its potential therapeutic applications.
Vulinacimab Biosimilar is a recombinant humanized IgG1 monoclonal antibody. It is composed of two heavy chains and two light chains, each with a molecular weight of approximately 50 kDa. The antibody has a unique binding site that specifically targets VEGFR2, which is a transmembrane receptor expressed on the surface of endothelial cells.
VEGFR2 is a key player in angiogenesis, the process of forming new blood vessels. It is activated by the binding of VEGF, a growth factor that promotes the growth and survival of endothelial cells. Vulinacimab Biosimilar works by binding to VEGFR2 and blocking the binding of VEGF, thereby inhibiting the downstream signaling pathways involved in angiogenesis. This ultimately leads to reduced blood vessel formation and disruption of the tumor microenvironment, which is crucial for the growth and spread of cancer cells.
Vulinacimab Biosimilar has shown potential in various pre-clinical studies as a therapeutic agent for cancer treatment. It has been evaluated in different tumor models, including breast, lung, and colon cancer, and has shown promising results in inhibiting tumor growth and metastasis. Additionally, Vulinacimab Biosimilar has also been studied in combination with other anti- cancer therapies, such as chemotherapy and radiation therapy, and has shown synergistic effects in enhancing their anti-tumor activity.
Currently, Vulinacimab Biosimilar is in the early stages of clinical development. Phase I clinical trials have been completed, and the results have shown favorable safety and tolerability profiles. The next step is to conduct Phase II clinical trials to evaluate the efficacy of Vulinacimab Biosimilar in cancer patients. These trials will also help determine the optimal dosage and schedule for the antibody.
With the promising results seen in pre-clinical studies and early clinical trials, Vulinacimab Biosimilar has the potential to be a valuable addition to the current arsenal of anti- cancer therapies. It has shown promise in inhibiting tumor growth and metastasis, and its combination with other therapies may further enhance its effectiveness. Further research and clinical trials will help determine the full potential of Vulinacimab Biosimilar as a therapeutic agent.
In summary, Vulinacimab Biosimilar is a monoclonal antibody that targets VEGFR2 and has shown potential as a therapeutic agent for cancer treatment. Its unique mechanism of action and promising results in pre-clinical studies make it a promising candidate for further development. As research and clinical trials continue, Vulinacimab Biosimilar may prove to be a valuable addition to the treatment options for cancer patients.
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