Human Hp CagA ELISA Kit

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  • Catalog
    E018110
  • species
    Human
  • GeneHp CagA
  • Standard CurveHuman Hp CagA ELISA Kit
  • Other Species Human HP-CAGA ELISA KitHuman HP CagA lgA ELISA KitMouse Hp-CagA ELISA KitMouse HP-CAGA-IgG ELISA KitMouse HP-CagA-lgA ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Hp-CagA. No significant cross-reactivity or interference between Hp-CagA and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between Hp-CagA 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 ng/mL.
  • Intended UseHuman Hp CagA ELISA Kit allows for the in vitro quantitative determination of Hp CagA , 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/FamilyMicrobiology
  • Product Description
    specifical
    Principle of the assay: Hp-CagA ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-Hp-CagA antibody and an Hp-CagA-HRP conjugate. The assay sample and buffer are incubated together with Hp-CagA-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 Hp-CagA concentration since Hp-CagA from samples and Hp-CagA-HRP conjugate compete for the anti-Hp-CagA antibody binding site. Since the number of sites is limited, as more sites are occupied by Hp-CagA from the sample, fewer sites are left to bind Hp-CagA-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The Hp-CagA concentration in each sample is interpolated from this standard curve.



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