Human APRIL ELISA Kit

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  • Alternative name

    Tumor necrosis factor ligand superfamily member 13 ELISA KIT; A proliferation-inducing ligand ELISA KIT; APRIL ELISA KIT; TNF- and APOL-related leukocyte expressed ligand 2 ELISA KIT; TALL-2 ELISA KIT; TNF-related death ligand 1 ELISA KIT; TRDL-1 ELISA KIT; CD_antigen: CD256TNFSF13 ELISA KIT; APRIL ELISA KIT; TALL2 ELISA KIT; ZTNF2 ELISA KIT; UNQ383/PRO715 ELISA KIT; APRIL ELISA KIT; TALL-2 ELISA KIT; TRDL-1 ELISA KIT

  • Catalog
    E000127
  • species
    Human
  • GeneAPRIL
  • Standard CurveHuman APRIL ELISA Kit
  • Other Species Human TNFSF13/APRIL ELISA KitMouse APRIL ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseHuman APRIL ELISA Kit allows for the in vitro quantitative determination of APRIL , 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: APRIL/CD256 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for APRIL/CD256. Standards or samples are then added to the microtiter plate wells and APRIL/CD256 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of APRIL/CD256 present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for APRIL/CD256 are added to each well to "sandwich" the APRIL/CD256 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 APRIL/CD256 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 APRIL/CD256 concentration in each sample is interpolated from this standard curve.


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