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Human DEFAlpha 5 ELISA Kit

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  • Alternative name

    Defensin-5 ELISA KIT; Defensin, alpha 5 ELISA KIT; HD5(20-94)Cleaved into the following 4 chains:HD5(23-94) ELISA KIT; HD5(29-94) ELISA KIT; HD5(56-94) ELISA KIT; HD5(63-94)DEFA5 ELISA KIT; DEF5 ELISA KIT
  • Catalog
    E011491
  • species
    Human
  • GeneDEFAlpha 5
  • Standard CurveHuman DEFAlpha 5 ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 pg/mL.
  • Intended UseHuman DEFAlpha 5 ELISA Kit allows for the in vitro quantitative determination of DEFAlpha 5 , 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    Intended Uses: This DEFa5 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human DEFa5. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: DEFa5 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for DEFa5. Standards or samples are then added to the microtiter plate wells and DEFa5 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of DEFa5 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for DEFa5 are added to each well to "sandwich" the DEFa5 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 DEFa5 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 DEFa5 concentration in each sample is interpolated from this standard curve.


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