Viral wnvNS3 Protease Antibody Summary
Ser1423-Lys1470, Gly1506-Leu1689
Accession # ABD85079
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of wnvNS3 Protease by Western Blot. Western blot shows lysates of Recombinant Viral wnvNS3 Protease. PVDF membrane was probed with 2 µg/mL of Mouse Anti-Viral wnvNS3 Protease Monoclonal Antibody (Catalog # MAB29071) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # HAF018). A specific band was detected for full length wnvNS3 Protease at approximately 32 kDa and C-terminal NS3 at approximately 22 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: wnvNS3 Protease
Infection of mosquito-borne West Nile Virus can cause severe neurological disease and can be epidemic. Two non-structural proteins, NS3 and NS2b, play an essential role in viral replication and are therefore a potential target for treatment and prevention of West Nile Virus disease. NS3 consists of a trypsin-like serine protease with a catalytic triad (His51, Asp75, Ser135) and a putative helicase. Requiring NS2b as the cofactor, NS3 protease processes viral polyprotein precursor (1, 2). The purified recombinant protein used as an immunogen consists of three forms: the full-length fusion protein, the N-terminal NS2b, and the C-terminal NS3 with a G4SG4 linker. NS3 protease has a relatively narrow substrate specificity that prefers Arg in P1 and Lys in P2.
Product Datasheets
Citations for Viral wnvNS3 Protease Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 3
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P-body components LSM1, GW182, DDX3, DDX6 and XRN1 are recruited to WNV replication sites and positively regulate viral replication
Authors: Harendra S. Chahar, Shuiping Chen, N. Manjunath
Virology
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West Nile virus infection causes endocytosis of a specific subset of tight junction membrane proteins.
Authors: Xu Z, Waeckerlin R, Urbanowski MD
PLoS ONE, 2012-05-24;7(5):e37886.
Species: Mouse
Sample Types: Whole Cells
Applications: ICC -
The capsid-binding nucleolar helicase DDX56 is important for infectivity of West Nile virus.
Authors: Xu Z, Anderson R, Hobman TC
J. Virol., 2011-03-16;85(11):5571-80.
Species: Human
Sample Types: Whole Cells
Applications: ICC
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