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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG4, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Denecimig Biosimilar - Anti-F9 and F10 mAb - Research Grade |
|---|---|
| Species | Homo sapiens |
| Expression system | XtenCHO |
| Purity | >90% by SDS-PAGE. |
| Buffer | 0.01M PBS, pH 7.4. |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | 4°C for short term; -20°C for long term |
| Brand | ProteoGenix |
| Aliases /Synonyms | anti-F9, Factor IX, F10, Factor X |
| Reference | PX-TA2059 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Denecimig Biosimilar – Anti-F9 and F10 mAb – Research Grade is a novel therapeutic antibody developed for the treatment of hemophilia. It is a biosimilar version of the existing anti-F9 and F10 monoclonal antibodies, which have shown promising results in clinical trials. This biosimilar version has been developed using advanced technology and has the potential to provide an effective and affordable treatment option for patients with hemophilia.
Denecimig Biosimilar – Anti-F9 and F10 mAb – Research Grade is a monoclonal antibody that specifically targets coagulation factors F9 and F10. It is a fully humanized antibody, meaning it is derived from human cells and has a similar structure to antibodies naturally produced in the body. This allows for better compatibility and reduces the risk of adverse reactions. The antibody consists of two heavy chains and two light chains, which are connected by disulfide bonds. It has a molecular weight of approximately 150 kDa.
The main function of Denecimig Biosimilar – Anti-F9 and F10 mAb – Research Grade is to inhibit the activity of coagulation factors F9 and F10. These factors are essential for the formation of blood clots and are deficient in patients with hemophilia. By binding to these factors, the antibody prevents them from participating in the clotting process, thereby reducing the risk of bleeding episodes. This mechanism of action is similar to that of the existing anti-F9 and F10 monoclonal antibodies, making Denecimig Biosimilar a promising treatment option for hemophilia patients.
The therapeutic target of Denecimig Biosimilar – Anti-F9 and F10 mAb – Research Grade is coagulation factors F9 and F10. These factors are responsible for the formation of blood clots, and their deficiency leads to the bleeding disorder known as hemophilia. By targeting these factors, the antibody helps to restore the balance of clotting and prevent bleeding episodes in patients with hemophilia. This makes it a highly specific and effective therapeutic agent for this condition.
Denecimig Biosimilar – Anti-F9 and F10 mAb – Research Grade is a high-quality antibody that has been developed for research purposes. It is produced using advanced technology and undergoes rigorous testing to ensure its purity and potency. This research grade version is primarily used for in vitro studies and pre-clinical trials to evaluate its safety and efficacy. It provides researchers with a valuable tool for studying the mechanism of action and potential therapeutic applications of this antibody.
Denecimig Biosimilar – Anti-F9 and F10 mAb – Research Grade has potential applications in the treatment of hemophilia. It can be used as a standalone therapy or in combination with other treatments to manage bleeding episodes and prevent complications in patients with hemophilia. Additionally, this antibody can also be used for research purposes to further understand the role of F9 and F10 in the clotting process and develop new treatments for hemophilia.
Denecimig Biosimilar – Anti-F9 and F10 mAb – Research Grade is a promising therapeutic antibody for the treatment of hemophilia. Its unique structure, mechanism of action, and specific targeting of coagulation factors F9 and F10 make it a highly effective and safe treatment option. Furthermore, its research grade version provides researchers with a valuable tool for studying the role of these factors in hemophilia and developing new treatments for this condition.
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