Human CD30L ELISA Kit

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  • Alternative name

    Tumor necrosis factor ligand superfamily member 8 ELISA KIT; CD30 ligand ELISA KIT; CD30-L ELISA KIT; CD_antigen: CD153TNFSF8 ELISA KIT; CD30L ELISA KIT; CD30LG ELISA KIT; CD30-L ELISA KIT

  • Catalog
    E007416
  • species
    Human
  • GeneCD30L
  • Standard CurveHuman CD30L ELISA Kit
  • Other Species Mouse CD30L ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of CD30L. No significant cross-reactivity or interference between CD30L and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between CD30L and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 pg/mL.
  • Intended UseHuman CD30L ELISA Kit allows for the in vitro quantitative determination of CD30L , 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: CD30L ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for CD30L. Standards or samples are then added to the microtiter plate wells and CD30L if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of CD30L present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for CD30L are added to each well to "sandwich" the CD30L 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 CD30L 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 CD30L concentration in each sample is interpolated from this standard curve.


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