Image of a kit SensoLyte 570 West Nile Virus Protease Assay Kit Fluorimetric
Assay-kits

SensoLyte® 570 West Nile Virus Protease Assay Kit Fluorimetric - 1 kit

€603.00
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  • Cat.Number : AS-72080
  • Availability :
    In production
  • Shipping conditions : Ice delivery fees must be applied

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West Nile virus (WNV) causes severe neurological disease and fatalities in both human and animal hosts. There is currently no effective vaccine or antiviral drug to protect against WNV infection. West Nile virus NS3 protease, essential for the proteolytic processing of the viral polyprotein precursor, is a promising target for the development of anti-WNV drugs.
The SensoLyte® 570 West Nile Virus Protease Assay Kit provides a convenient homogeneous assay for high throughput screening of WNV protease inhibitors and for continuous assay of NS3 protease activity using QXL™570/5-TAMRA FRET substrate. Upon cleavage into two separate fragments by the WNV NS3 protease, the fluorescence of 5-TAMRA can be monitored at excitation/emission = 540 nm/575 nm.

Specifications

Packaging
Kits components
  • Component A: QXL™570/5-TAMRA, WNV protease substrate, Ex/Em=540 nm/575 nm: 1.5 mM DMSO solution, 60 µL Component B: 5-TAMRA, fluorescence reference standard, Ex/Em=540 nm/575 nm: 750 µM DMSO solution, 10 µL Component C: Assay Buffer: 20 mL Component D: WNV Protease Inhibitor undeca-D-Arg-NH2: 1 mM DMSO solution, 10 µL
Properties
Absorbance (nm)
  • 540
Emission (nm)
  • 575
Storage & stability
Storage Conditions
  • Store all kit components at -20°C. Protect Components A and B from light and from moisture. Component C can be stored at room temperature for convenience.
Activity
Application
Biomarker Target
Detection Method
Research Area
Sub-category Research Area
Usage
  • Research use
Codes
Code Nacres
  • NA.32

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Citations

Kinetic analysis of the inhibition of matrix metalloproteinases: lessons from the study of tissue inhibitors of metalloproteinases.

Methods Mol Biol. . 2010 Jan 01 ; 622 435 | DOI : 10.1007/978-1-60327-299-5_25

  • F. Willenbrock
  • et al