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  • Catalog
  • species
  • Standard CurveMouse AGPA ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of GPCAb. No significant cross-reactivity or interference between GPCAb and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between GPCAb 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 AGPA ELISA Kit allows for the in vitro quantitative determination of , 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
    Intended Uses: This GPCAb ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse GPCAb. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay||GPCAb ELISA kit applies the competitive enzyme immunoassay technique utilizing Gastric Parietal cell antigen and an GPCAb-HRP conjugate. The assay sample and buffer are incubated together with GPCAb-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 GPCAb concentration since GPCAb from samples and GPCAb-HRP conjugate compete for the Gastric Parietal cell antigen binding site. Since the number of sites is limited, as more sites are occupied by GPCAb from the sample, fewer sites are left to bind GPCAb-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The GPCAb concentration in each sample is interpolated from this standard curve.

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