Mouse RI ELISA Kit

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  • Alternative name

    Ribonuclease inhibitor ELISA KIT; Placental ribonuclease inhibitor ELISA KIT; Placental RNase inhibitor ELISA KIT; Ribonuclease/angiogenin inhibitor 1 ELISA KIT; RAIRNH1 ELISA KIT; PRI ELISA KIT; RNH ELISA KIT; Placental RNase inhibitor ELISA KIT; RAI ELISA KIT

  • Catalog
    E066538
  • species
    Mouse
  • GeneRI
  • Standard CurveMouse RI ELISA Kit
  • Other Species Human ANNA-2 / Ri ELISA KitHuman ANNA-2/Ri ELISA KitHuman RI ELISA KitMouse AT II RI ELISA KitMouse ANNA-2 / Ri ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of RI. No significant cross-reactivity or interference between RI and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between RI and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseMouse RI ELISA Kit allows for the in vitro quantitative determination of RI , 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/FamilyCell Biology
  • Product Description
    specifical
    Principle of the assay: RI ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-RI antibody and an RI-HRP conjugate. The assay sample and buffer are incubated together with RI-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 RI concentration since RI from samples and RI-HRP conjugate compete for the anti-RI antibody binding site. Since the number of sites is limited, as more sites are occupied by RI from the sample, fewer sites are left to bind RI-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The RI concentration in each sample is interpolated from this standard curve.



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