Mouse PVRL2 ELISA Kit

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  • Alternative name

    Nectin-2 ELISA KIT; Herpes virus entry mediator B ELISA KIT; Herpesvirus entry mediator B ELISA KIT; HveB ELISA KIT; Poliovirus receptor-related protein 2 ELISA KIT; CD_antigen: CD112PVRL2 ELISA KIT; HVEB ELISA KIT; PRR2 ELISA KIT; Herpesvirus entry mediator B ELISA KIT; HveB ELISA KIT

  • Catalog
    E065613
  • species
    Mouse
  • GenePVRL2
  • SpecificityThis kit recognizes natural and recombinant Mouse PVRL2. No significant cross-reactivity or interference between Mouse PVRL2 and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of Mouse PVRL2 is 46.875pg/mL (The sensitivity of this assay, or lowest detectable limit (LDL) was defined as the lowest protein concentration that could be differentiated from zero).
  • Intended UseMouse PVRL2 ELISA Kit allows for the in vitro quantitative determination of PVRL2 , 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 Description
    specifical
    Principle of the assay: This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to PVRL2. Standards or samples are added to the appropriate micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for PVRL2 and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain PVRL2, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of PVRL2. You can calculate the concentration of PVRL2 in the samples by comparing the OD of the samples to the standard curve.



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