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