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| Size | 100ug, 1MG |
|---|---|
| Isotype | [(scFv-heavy-kappa)-IGHE-CH4]2 |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Radretumab Biosimilar - Anti-FN EDB mAb - Research Grade |
|---|---|
| Source | CAS 1253180-81-2 |
| Species | Homo sapiens |
| Expression system | Mammalian cells |
| 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 | Radretumab,L19-131 I,L19-SIP,FN EDB,anti-FN EDB |
| Reference | PX-TA1262 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | [(scFv-heavy-kappa)-IGHE-CH4]2 |
| Clonality | Monoclonal Antibody |
Radretumab Biosimilar – Anti-FN EDB mAb is a promising therapeutic agent that has gained significant attention in recent years due to its potential in treating cancer and other diseases. This biosimilar is a monoclonal antibody that specifically targets the fibronectin extra domain B (FN EDB), a protein that is overexpressed in various types of cancers and plays a crucial role in tumor growth and metastasis. In this article, we will delve deeper into the structure, activity, and potential applications of this novel biosimilar.
Radretumab Biosimilar is a recombinant, humanized monoclonal antibody that is produced by using advanced genetic engineering techniques. It is a biosimilar of the original Radretumab, which was developed by a Japanese biopharmaceutical company. The biosimilar is designed to have a similar structure and function as the original drug, but at a lower cost. The antibody consists of two identical heavy chains and two identical light chains, each with a molecular weight of approximately 150 kDa. These chains are connected by disulfide bonds and form a Y-shaped structure, with the antigen-binding sites located at the tips of the arms.
The main mechanism of action of Radretumab Biosimilar is its ability to bind to the FN EDB protein with high specificity and affinity. FN EDB is a splicing variant of the fibronectin protein, which is involved in cell adhesion, migration, and tissue repair. However, in cancer cells, FN EDB is overexpressed and plays a critical role in promoting tumor growth and metastasis. By binding to FN EDB, Radretumab Biosimilar blocks its activity and inhibits the growth and spread of cancer cells.
The potential applications of Radretumab Biosimilar are vast, and ongoing research is exploring its use in various diseases, especially cancer. Some of the potential therapeutic targets of this biosimilar include:
1. Solid Tumors: FN EDB is highly expressed in various solid tumors, including breast, lung, colon, and pancreatic cancers. Radretumab Biosimilar has shown promising results in preclinical studies as a potential treatment for these cancers.
2. Angiogenesis: FN EDB is involved in the formation of new blood vessels, a process known as angiogenesis, which is essential for tumor growth. By inhibiting FN EDB, Radretumab Biosimilar can potentially block angiogenesis and slow down tumor growth.
3. Metastasis: FN EDB is also known to play a crucial role in the spread of cancer to other parts of the body. By targeting FN EDB, Radretumab Biosimilar has the potential to inhibit metastasis and improve patient outcomes.
4. Inflammation: FN EDB is also involved in the inflammatory response, and its overexpression has been linked to various inflammatory diseases. Radretumab Biosimilar has shown promising results in preclinical studies as a potential treatment for these conditions.
Apart from its therapeutic potential, Radretumab Biosimilar is also widely used in research as a tool to study the role of FN EDB in various diseases. Its high specificity and affinity make it a valuable tool for detecting and quantifying FN EDB expression in tissues and cells. This biosimilar is also used in preclinical studies to evaluate its efficacy and safety in different disease models.
In conclusion, Radretumab Biosimilar – Anti-FN EDB mAb is a promising therapeutic agent with a well-defined structure and mechanism of action. Its potential applications in treating cancer and other diseases make it a valuable addition to the field of biopharmaceuticals. Ongoing research and clinical trials will provide further insights into the efficacy and safety of this biosimilar, and it is expected to play a significant role in improving patient outcomes in the future.
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