Anti-RSV Antibody Fab (MOM-18098-F(E))
|Recombinant Anti-RSV Antibody Fab Fragment
- Product Overview
- Recombinant Humanized (from mouse) Antibody Fab Fragment binds selectively to respiratory syncytial virus, expressed in Chinese Hamster Ovary cells(CHO)
- respiratory syncytial virus
- Fab Fragment based on Humanized (from mouse) IgG1 - kappa
- Suitable for use in FC, IP, ELISA, Neut, FuncS, IF and most other immunological methods.
- Predicted N terminal
- H chain: QVQLVQS; L Chain: DIQMTQS
- Purity >95% by SDS-PAGE.
- Store at -20°C. Avoid multiple freeze/thaw cycles.
- Monoclonal Antibody binds to the fusion glycoprotein of RSV. Against respiratory syncytial virus.
- Antigen Description
- Respiratory Syncytial Virus (RSV) Fusion (F) Glycoprotein is a Class I viral fusion protein. Under the current model, the protein has at least 3 conformational states: pre-fusion native state, pre-hairpin intermediate state, and post-fusion hairpin state. During viral and target cell membrane fusion, the heptad repeat (HR) regions assume a trimer-of-hairpins structure, positioning the fusion peptide in close proximity to the C-terminal region of the ectodomain. The formation of this structure appears to drive apposition and subsequent fusion of viral and target cell membranes. Directs fusion of viral and cellular membranes leading to delivery of the nucleocapsid into the cytoplasm. This fusion is pH independent and occurs directly at the outer cell membrane. The trimer of F1-F2 (protein F) interacts with glycoprotein G at the virion surface. Upon binding of G to heparan sulfate, the hydrophobic fusion peptide is unmasked and interacts with the cellular membrane, inducing the fusion between host cell and virion membranes. Notably, RSV fusion protein is able to interact directly with heparan sulfate and therefore actively participates in virus attachment. Furthermore, the F2 subunit was identifed as the major determinant of RSV host cell specificity. Later in infection, proteins F expressed at the plasma membrane of infected cells mediate fusion with adjacent cells to form syncytia, a cytopathic effect that could lead to tissue necrosis. The fusion protein is also able to trigger p53-dependent apoptosis.
- RSV Fusion F Glycoprotein; RSV; Respiratory Syncytial Virus
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