Mouse CYP17 ELISA Kit

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  • Alternative name

    Steroid 17-alpha-hydroxylase/17,20 lyase ELISA KIT; CYPXVII ELISA KIT; Cytochrome P450 17A1 ELISA KIT; Cytochrome P450-C17 ELISA KIT; Cytochrome P450c17 ELISA KIT; Steroid 17-alpha-monooxygenaseCYP17A1 ELISA KIT; CYP17 ELISA KIT; S17AH ELISA KIT

  • Catalog
    E050278
  • species
    Mouse
  • GeneCYP17
  • Standard CurveMouse CYP17 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of CYP-17alpha. No significant cross-reactivity or interference between CYP-17alpha and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between CYP-17alpha and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 pg/mL.
  • Intended UseMouse CYP17 ELISA Kit allows for the in vitro quantitative determination of CYP17 , 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 Categories/FamilyMouse ELISA Kit
  • Product Description
    specifical
    Principle of the assay: CYP-17alpha ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-CYP-17alpha antibody and an CYP-17alpha-HRP conjugate. The assay sample and buffer are incubated together with CYP-17alpha-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the CYP-17alpha concentration since CYP-17alpha from samples and CYP-17alpha-HRP conjugate compete for the anti-CYP-17alpha antibody binding site. Since the number of sites is limited, as more sites are occupied by CYP-17alpha from the sample, fewer sites are left to bind CYP-17alpha-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The CYP-17alpha concentration in each sample is interpolated from this standard curve.



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