Human uPAR ELISA Kit

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  • Alternative name

    Urokinase plasminogen activator surface receptor ELISA KIT; Monocyte activation antigen Mo3 ELISA KIT; CD_antigen: CD87PLAUR ELISA KIT; MO3 ELISA KIT; UPAR ELISA KIT; U-PAR ELISA KIT; uPAR ELISA KIT

  • Catalog
    E029619
  • species
    Human
  • GeneuPAR
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Plasminogen Activator, Urokinase Receptor (uPAR). No significant cross-reactivity or interference between Plasminogen Activator, Urokinase Receptor (uPAR) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.069ng/mL.
  • Intended UseHuman uPAR ELISA Kit allows for the in vitro quantitative determination of uPAR , 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 Plasminogen Activator, Urokinase Receptor (uPAR). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Plasminogen Activator, Urokinase Receptor (uPAR). 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 Receptor (uPAR), 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 Receptor (uPAR) in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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