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Human ALP ELISA Kit

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  • Alternative name

    Alkaline phosphatase, tissue-nonspecific isozyme ELISA KIT; Alkaline phosphatase liver/bone/kidney isozymeALPL ELISA KIT; AP-TNAP ELISA KIT; TNSALP ELISA KIT
  • Catalog
    E001380
  • species
    Human
  • GeneALP
  • Standard CurveHuman ALP ELISA Kit
  • Other Species Human ALP-B ELISA KitMouse ALP ELISA KitMouse ALP-B ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Alkaline Phosphatase (ALP). No significant cross-reactivity or interference between Alkaline Phosphatase (ALP) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.284ng/mL.
  • Intended UseHuman ALP ELISA Kit allows for the in vitro quantitative determination of ALP , 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 Alkaline Phosphatase (ALP). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Alkaline Phosphatase (ALP). 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 Alkaline Phosphatase (ALP), 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 Alkaline Phosphatase (ALP) in the samples is then determined by comparing the O.D. of the samples to the standard curve.


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