Human OIT3 ELISA Kit

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  • Alternative name

    Oncoprotein-induced transcript 3 protein ELISA KIT; Liver-specific zona pellucida domain-containing proteinOIT3 ELISA KIT; LZP ELISA KIT

  • Catalog
    E027683
  • species
    Human
  • GeneOIT3
  • Standard CurveHuman OIT3 ELISA Kit
  • Other Species Mouse Oit3 ELISA KitBovine OIT3 ELISA KitRat Oit3 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of OIT3. No significant cross-reactivity or interference between OIT3 and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of human OIT3 is typically less than 0.109ng/mL. The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined by addi
  • Intended UseHuman OIT3 ELISA Kit allows for the in vitro quantitative determination of OIT3 , 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 microtiter plate provided in this kit has been pre-coated with an antibody specific to OIT3. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to OIT3. 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 OIT3, 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 OIT3 in the samples is then determined by comparing the O.D. of the samples to the standard curve.


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