Human caspase 9 ELISA Kit

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  • Alternative name

    Caspase-9 ELISA KIT; Apoptotic protease Mch-6 ELISA KIT; Apoptotic protease-activating factor 3 ELISA KIT; APAF-3 ELISA KIT; ICE-like apoptotic protease 6 ELISA KIT; ICE-LAP6CASP9 ELISA KIT; MCH6 ELISA KIT; CASP-9 ELISA KIT; APAF-3 ELISA KIT; ICE-LAP6 ELISA KIT

  • Catalog
  • species
  • Genecaspase 9
  • Standard CurveHuman caspase 9 ELISA Kit
  • Other Species Human Caspase-9/MCH6/ICE-LAP6 ELISA KitMouse caspase-9 ELISA KitMouse Caspase-9/MCH6/ICE-LAP6 ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 ng/mL.
  • Intended UseHuman caspase 9 ELISA Kit allows for the in vitro quantitative determination of caspase 9 , 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/FamilyCell Biology
  • Product Description
    Principle of the Assay: caspase-9 ELISA kit applies the quantitative sandwich enzyme irnmunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for caspase-9. Standards or samples are then added to the microtiter plate wells and caspase-9 if present, will bind to the antibody pre-coated wells, hi order to quantitatively determine the amount of caspase-9 present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for caspase-9 are added to each well to "sandwich" the caspase-9 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 caspase-9 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 caspase-9 concentration in each sample is interpolated from this standard curve.

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