Human HNF1beta ELISA Kit

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  • Alternative name

    Hepatocyte nuclear factor 1-beta ELISA KIT; Homeoprotein LFB3 ELISA KIT; Transcription factor 2 ELISA KIT; TCF-2 ELISA KIT; Variant hepatic nuclear factor 1 ELISA KIT; vHNF1HNF1B ELISA KIT; TCF2 ELISA KIT; HNF-1-beta ELISA KIT; HNF-1B ELISA KIT; TCF-2 ELISA KIT; vHNF1 ELISA KIT

  • Catalog
    E018398
  • species
    Human
  • GeneHNF1beta
  • Standard CurveHuman HNF1beta ELISA Kit
  • Other Species Mouse HNF1beta ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Intended UseHuman HNF1beta ELISA Kit allows for the in vitro quantitative determination of HNF1beta , 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
    specifical
    Intended Uses: This HNF1B 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 ofHNF1B in the sample, thisHNF1B 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 versusHNF1B concentration. The concentration ofHNF1B in the samples is then determined by comparing the O.D. of the samples to the standard curve. Principle of the Assay: This HNF1B 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 forHNF1B. Standards or samples are then added to the microtiter plate wells andHNF1B if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount ofHNF1B present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific forHNF1B are added to each well to "sandwich" theHNF1B 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 containHNF1B 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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