Mouse SPINK5 ELISA Kit

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  • Alternative name

    Serine protease inhibitor Kazal-type 5 ELISA KIT; Lympho-epithelial Kazal-type-related inhibitor ELISA KIT; LEKTISPINK5 ELISA KIT; LEKTI ELISA KIT

  • Catalog
    E067345
  • species
    Mouse
  • GeneSPINK5
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Serine Peptidase Inhibitor Kazal Type 5 (SPINK5). No significant cross-reactivity or interference between Serine Peptidase Inhibitor Kazal Type 5 (SPINK5) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 29pg/mL.
  • Intended UseMouse SPINK5 ELISA Kit allows for the in vitro quantitative determination of SPINK5 , 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 Serine Peptidase Inhibitor Kazal Type 5 (SPINK5). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Serine Peptidase Inhibitor Kazal Type 5 (SPINK5). 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 Serine Peptidase Inhibitor Kazal Type 5 (SPINK5), 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 Serine Peptidase Inhibitor Kazal Type 5 (SPINK5) in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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