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  • Alternative name

    Nucleosome assembly protein 1-like 1 ELISA KIT; NAP-1-related protein ELISA KIT; hNRPNAP1L1 ELISA KIT; NRP ELISA KIT; hNRP ELISA KIT

  • Catalog
  • species
  • GeneNAP
  • Standard CurveHuman NAP ELISA Kit
  • Other Species Human IL-8/NAP-1 ELISA KitHuman NAP 2 ELISA KitHuman NAP-2 ELISA KitMouse NAP-2/CXCL7 ELISA KitMouse NAP-2 ELISA KitMouse NAP ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Neutrophil Alkaline Phosphatase (NAP). No significant cross-reactivity or interference between Neutrophil Alkaline Phosphatase (NAP) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.57ng/mL.
  • Intended UseHuman NAP ELISA Kit allows for the in vitro quantitative determination of NAP , 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
    Principle of the Assay: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Neutrophil Alkaline Phosphatase (NAP). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Neutrophil Alkaline Phosphatase (NAP). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Neutrophil Alkaline Phosphatase (NAP), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Neutrophil Alkaline Phosphatase (NAP) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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