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Mouse ACH ELISA Kit

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  • Catalog
    E042427
  • species
    Mouse
  • GeneACH
  • Standard CurveMouse ACH ELISA Kit
  • Other Species Human ACH ELISA KitHuman ACh ELISA KitBovine ACH ELISA KitCanine ACH ELISA KitChicken ACH ELISA KitGeneral ACH ELISA KitPorcine ACH ELISA KitRabbit ACH ELISA KitRat ACH ELISA KitCamel ACH ELISA KitGoat ACH ELISA KitGuinea Pig ACH ELISA KitHamster ACH ELISA KitHorse ACH ELISA KitMonkey ACH ELISA KitSheep ACH ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of ACH. No significant cross-reactivity or interference between ACH and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between ACH 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 ACH ELISA Kit allows for the in vitro quantitative determination of ACH , 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
    specifical    Principle of the assay: ACH ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-ACH antibody and an ACH-HRP conjugate. The assay sample and buffer are incubated together with ACH-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 ACH concentration since ACH from samples and ACH-HRP conjugate compete for the anti-ACH antibody binding site. Since the number of sites is limited, as more sites are occupied by ACH from the sample, fewer sites are left to bind ACH-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ACH concentration in each sample is interpolated from this standard curve.



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