Human OT ELISA Kit

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  • Alternative name

    Oxytocin ELISA KIT; OxytocinOxt ELISA KIT;

  • Catalog
  • species
  • GeneOT
  • Standard CurveHuman OT ELISA Kit
  • Other Species Human N MID OT ELISA KitHuman N-MID-OT ELISA KitHuman OT/BGP ELISA KitHuman OT ELISA KitMouse OT/BGP ELISA KitMouse OT ELISA KitBovine OT ELISA KitCanine OT ELISA KitChicken OT ELISA KitGeneral OT ELISA KitPorcine OT ELISA KitRabbit OT ELISA KitRat OT ELISA KitCamel OT ELISA KitGoat OT ELISA KitGuinea Pig OT ELISA KitHamster OT ELISA KitHorse OT ELISA KitMonkey OT ELISA KitSheep OT ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of OT. No significant cross-reactivity or interference between OT and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between OT 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 UseHuman OT ELISA Kit allows for the in vitro quantitative determination of OT , 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: OT ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-OT antibody and an OT-HRP conjugate. The assay sample and buffer are incubated together with OT-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 OT concentration since OT from samples and OT-HRP conjugate compete for the anti-OT antibody binding site. Since the number of sites is limited, as more sites are occupied by OT from the sample, fewer sites are left to bind OT-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The OT concentration in each sample is interpolated from this standard curve.

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