Mouse GluAP ELISA Kit

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  • Alternative name

    Glutamyl aminopeptidase ELISA KIT; Aminopeptidase A ELISA KIT; AP-A ELISA KIT; Differentiation antigen gp160 ELISA KIT; CD_antigen: CD249ENPEP ELISA KIT; EAP ELISA KIT; AP-A ELISA KIT

  • Catalog
    E054446
  • species
    Mouse
  • GeneGluAP
  • Standard CurveMouse GluAP ELISA Kit
  • Other Species Human GluAP ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Glutamyl Aminopeptidase (GluAP). No significant cross-reactivity or interference between Glutamyl Aminopeptidase (GluAP) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.062ng/mL.
  • Intended UseMouse GluAP ELISA Kit allows for the in vitro quantitative determination of GluAP , 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: 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 Glutamyl Aminopeptidase (GluAP). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Glutamyl Aminopeptidase (GluAP). 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 Glutamyl Aminopeptidase (GluAP), 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 Glutamyl Aminopeptidase (GluAP) in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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