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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Felvizumab Biosimilar - Anti-RSV mAb - Research Grade |
|---|---|
| Source | CAS 167747-20-8 |
| 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 | Felvizumab,SB 209763,RSV,anti-RSV |
| Reference | PX-TA1061 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Felvizumab Biosimilar – Anti-RSV mAb – Research Grade: A Promising Antibody for RSV Treatment Felvizumab biosimilar, also known as anti-RSV mAb, is a monoclonal antibody that has shown great potential in the treatment of respiratory syncytial virus (RSV) infection. This biosimilar is a research grade product that is currently in the pre-clinical stage of development. In this article, we will delve into the structure, activity, and potential applications of Felvizumab biosimilar as a therapeutic target for RSV.
Felvizumab biosimilar is a monoclonal antibody that is designed to mimic the structure of the original Felvizumab, a humanized monoclonal antibody that targets the fusion protein of RSV. It is composed of two identical heavy chains and two identical light chains, connected by disulfide bonds. The heavy chains consist of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chains have two constant domains (CL and CL1) and one variable domain (VL). The variable domains are responsible for binding to the RSV fusion protein, while the constant domains play a role in effector functions.
Felvizumab biosimilar works by binding to the fusion protein of RSV, which is essential for viral entry into host cells. By binding to this protein, Felvizumab blocks the fusion process and prevents the virus from infecting cells. In addition, this biosimilar also activates the immune system to clear the virus from the body. The constant domains of Felvizumab biosimilar interact with immune cells, such as natural killer cells and macrophages, to trigger antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC). These effector functions help in the elimination of infected cells and control the spread of the virus.
The primary application of Felvizumab biosimilar is in the treatment of RSV infection. RSV is a common respiratory virus that can cause severe illness, especially in infants, young children, and older adults. Currently, there is no specific treatment for RSV, and management is limited to supportive care. However, with the development of Felvizumab biosimilar, there is hope for a targeted and effective therapy for RSV.
In addition to its use as a therapeutic agent, Felvizumab biosimilar also has potential applications in research and development. It can be used as a tool in studies investigating the role of RSV fusion protein in viral entry and pathogenesis. Furthermore, this biosimilar can serve as a reference material for the development and validation of RSV diagnostic assays.
Felvizumab biosimilar, also known as anti-RSV mAb, is a promising antibody for the treatment of RSV infection. Its structure, activity, and potential applications make it a valuable asset in the fight against this common respiratory virus. With ongoing research and development, Felvizumab biosimilar has the potential to provide a targeted and effective therapy for RSV, improving outcomes for those affected by this virus.
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