Human Gzms A ELISA Kit

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  • Alternative name

    Granzyme A ELISA KIT; CTL tryptase ELISA KIT; Cytotoxic T-lymphocyte proteinase 1 ELISA KIT; Fragmentin-1 ELISA KIT; Granzyme-1 ELISA KIT; Hanukkah factor ELISA KIT; H factor ELISA KIT; HFGZMA ELISA KIT; CTLA3 ELISA KIT; HFSP ELISA KIT; H factor ELISA KIT; HF ELISA KIT

  • Catalog
    E017449
  • species
    Human
  • GeneGzms A
  • Standard CurveHuman Gzms A ELISA Kit
  • Other Species Mouse Gzms-A ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 pg/mL.
  • Intended UseHuman Gzms A ELISA Kit allows for the in vitro quantitative determination of Gzms A , 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/FamilyImmunology
  • Product Description
    specifical
    Principle of the Assay: Gzms-A ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for Gzms-A. Standards or samples are then added to the microtiter plate wells and Gzms-A if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of Gzms-A present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for Gzms-A are added to each well to "sandwich" the Gzms-A 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 Gzms-A 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 Gzms-A concentration in each sample is interpolated from this standard curve.


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