Human AP13 ELISA Kit

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  • Catalog
    E003212
  • species
    Human
  • GeneAP13
  • Standard CurveHuman AP13 ELISA Kit
  • Other Species Mouse AP13 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Apelin-13. No significant cross-reactivity or interference between Apelin-13 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between Apelin-13 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 UseHuman AP13 ELISA Kit allows for the in vitro quantitative determination of AP13 , 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/FamilyHuman ELISA Kit
  • Product Description
    specifical
    Principle of the assay: Apelin-13 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for Apelin-13. Standards or samples are then added to the microtiter plate wells and Apelin-13 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of Apelin-13 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for Apelin-13 are added to each well to "sandwich" the Apelin-13 immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain Apelin-13 and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The Apelin-13 concentration in each sample is interpolated from this standard curve.


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