Human uPA ELISA Kit

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  • Alternative name

    Urokinase-type plasminogen activator ELISA KIT; PLAU ELISA KIT; U-plasminogen activator ELISA KIT; uPA ELISA KIT

  • Catalog
  • species
  • GeneuPA
  • Standard CurveHuman uPA ELISA Kit
  • Other Species Human PLAU/uPA ELISA KitMouse uPA ELISA KitMouse PLAU/uPA ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Plasminogen Activator, Urokinase (uPA). No significant cross-reactivity or interference between Plasminogen Activator, Urokinase (uPA) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 6.1pg/mL.
  • Intended UseHuman uPA ELISA Kit allows for the in vitro quantitative determination of uPA , 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 Plasminogen Activator, Urokinase (uPA). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Plasminogen Activator, Urokinase (uPA). 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 Plasminogen Activator, Urokinase (uPA), 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 Plasminogen Activator, Urokinase (uPA) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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