Human C/EBPbeta ELISA Kit

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  • Alternative name

    CCAAT/enhancer-binding protein beta ELISA KIT; Liver activator protein ELISA KIT; LAP ELISA KIT; Liver-enriched inhibitory protein ELISA KIT; LIP ELISA KIT; Nuclear factor NF-IL6 ELISA KIT; Transcription factor 5 ELISA KIT; TCF-5CEBPB ELISA KIT; TCF5 ELISA KIT; PP9092 ELISA KIT; C/EBP beta ELISA KIT; LAP ELISA KIT; LIP ELISA KIT; TCF-5 ELISA KIT

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

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