Human ELA2 ELISA Kit

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  • Alternative name

    Neutrophil elastase ELISA KIT; Bone marrow serine protease ELISA KIT; Elastase-2 ELISA KIT; Human leukocyte elastase ELISA KIT; HLE ELISA KIT; Medullasin ELISA KIT; PMN elastaseELANE ELISA KIT; ELA2 ELISA KIT; HLE ELISA KIT

  • Catalog
  • species
  • GeneELA2
  • Standard CurveHuman ELA2 ELISA Kit
  • Other Species Human NE/ELA2 ELISA KitMouse ELA2 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Elastase 2, Neutrophil (ELA2). No significant cross-reactivity or interference between Elastase 2, Neutrophil (ELA2) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.08ng/mL.
  • Intended UseHuman ELA2 ELISA Kit allows for the in vitro quantitative determination of ELA2 , 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 Elastase 2, Neutrophil (ELA2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Elastase 2, Neutrophil (ELA2). 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 Elastase 2, Neutrophil (ELA2), 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 Elastase 2, Neutrophil (ELA2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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