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| Size | 100µg, 1MG |
|---|---|
| Isotype | IgG4, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Sirexatamab Biosimilar - Anti-Dickkopf-1 mAb - Research Grade |
|---|---|
| Source | CAS: 2414962-49-3 |
| Species | Humanized |
| 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 | Sirexatamab,DKN-01, LY-2812176,Dickkopf-1,anti-Dickkopf-1 |
| Reference | PX-TA1779 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Sirexatamab Biosimilar, also known as Anti-Dickkopf-1 mAb, is a novel antibody that has shown promising results in pre-clinical and clinical studies. This biosimilar is designed to target a specific protein called Dickkopf-1 (DKK1), which has been found to play a crucial role in the development and progression of various diseases. In this article, we will discuss the structure, activity, and potential applications of Sirexatamab Biosimilar as a therapeutic agent.
Sirexatamab Biosimilar is a monoclonal antibody, meaning it is produced from a single clone of immune cells. It is a fully humanized antibody, which means that it is derived from human cells and has a structure similar to natural human antibodies. The antibody consists of two heavy chains and two light chains, connected by disulfide bonds. The heavy chains contain a constant region and a variable region, while the light chains only have a variable region. The variable regions are responsible for binding to the target protein, DKK1.
The main activity of Sirexatamab Biosimilar is to bind to DKK1 and inhibit its function. DKK1 is a secreted protein that acts as an antagonist of the Wnt signaling pathway. This pathway plays a crucial role in cell growth, differentiation, and survival. By binding to DKK1, Sirexatamab Biosimilar prevents it from interacting with its receptors and inhibits the Wnt signaling pathway. This, in turn, leads to a decrease in cell proliferation and survival, making it a potential therapeutic target for various diseases.
Sirexatamab Biosimilar has shown promising results in pre-clinical studies as a potential treatment for multiple myeloma, a type of blood cancer. In a phase I clinical trial, it was found to be well-tolerated and showed promising efficacy in patients with relapsed or refractory multiple myeloma. The biosimilar is also being investigated as a potential treatment for other types of cancer, such as solid tumors and hematologic malignancies.
In addition to its potential as a cancer treatment, Sirexatamab Biosimilar has also shown promise in the treatment of other diseases. DKK1 has been found to play a role in bone metabolism, and its inhibition has been linked to an increase in bone formation. This makes Sirexatamab Biosimilar a potential treatment for bone-related diseases, such as osteoporosis and bone metastases.
Furthermore, DKK1 has been implicated in autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus. By inhibiting DKK1, Sirexatamab Biosimilar may have potential as a treatment for these conditions as well.
In summary, Sirexatamab Biosimilar, also known as Anti-Dickkopf-1 mAb, is a novel monoclonal antibody with a unique structure and mechanism of action. It binds to DKK1 and inhibits its function, making it a potential therapeutic target for various diseases. Its promising results in pre-clinical and clinical studies make it a promising candidate for the treatment of cancer, bone-related diseases, and autoimmune disorders. Further research and clinical trials are needed to fully explore the potential of this biosimilar as a therapeutic agent.
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