Human c Jun ELISA Kit

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  • Alternative name

    Transcription factor AP-1 ELISA KIT; Activator protein 1 ELISA KIT; AP1 ELISA KIT; Proto-oncogene c-Jun ELISA KIT; V-jun avian sarcoma virus 17 oncogene homologJUN ELISA KIT; AP1 ELISA KIT

  • Catalog
  • species
  • Genec Jun
  • Standard CurveHuman c Jun ELISA Kit
  • Other Species Human C-jun ELISA KitMouse c-jun ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Intended UseHuman c Jun ELISA Kit allows for the in vitro quantitative determination of c Jun , 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/FamilyCardiovascular
  • Product Description
    Intended Uses: This C-JUN ELISA kit is intended Laboratory for research use only and is not for use in diagnostic or therapeutic procedures.The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration ofC-JUN in the sample, thisC-JUN ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versusC-JUN concentration. The concentration ofC-JUN in the samples is then determined by comparing the O.D. of the samples to the standard curve. Principle of the Assay: This C-JUN enzyme linked immunosorbent assay applies a technique called a quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific forC-JUN. Standards or samples are then added to the microtiter plate wells andC-JUN if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount ofC-JUN present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific forC-JUN are added to each well to "sandwich" theC-JUN immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, A and B substrate solution is added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period.Only those wells that containC-JUN and enzyme-conjugated antibody will exhibit a change in colour. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the colour change is measured spectrophotometrically at a wavelength of 450 nm.

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