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  • GeneVWF
  • Standard CurveMouse VWF ELISA Kit
  • Other Species Human ADAMTS13/vWF cp ELISA KitHuman ADAMTS-13 / vWF-cp ELISA KitHuman ADAMTS-13/vWF-cp ELISA KitHuman VWF ELISA KitMouse VWF-CP ELISA KitMouse ADAMTS13/vWF-cp ELISA KitMouse ADAMTS-13 / vWF-cp ELISA KitBovine VWF ELISA KitPorcine VWF ELISA KitRat Vwf ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of vWF. No significant cross-reactivity or interference between vWF and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between vWF and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseMouse VWF ELISA Kit allows for the in vitro quantitative determination of VWF , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageFor 5-7days:Store the whole kit at 4℃
    For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
  • Product Categories/FamilyMouse ELISA Kit
  • Product Description
    Intended Uses: This vWF ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse vWF. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay||VWF ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-vWF antibody and an vWF-HRP conjugate. The assay sample and buffer are incubated together with vWF-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the vWF concentration since vWF from samples and vWF-HRP conjugate compete for the anti-vWF antibody binding site. Since the number of sites is limited, as more sites are occupied by vWF from the sample, fewer sites are left to bind vWF-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The vWF concentration in each sample is interpolated from this standard curve.

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