Human MR ELISA Kit

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  • Alternative name

    Mineralocorticoid receptor ELISA KIT; Nuclear receptor subfamily 3 group C member 2NR3C2 ELISA KIT; MCR ELISA KIT; MLR ELISA KIT; MR ELISA KIT

  • Catalog
  • species
  • GeneMR
  • Standard CurveHuman MR ELISA Kit
  • Other Species Human MR-proANP ELISA KitHuman MR proANP ELISA KitMouse MR-proANP ELISA KitMouse MR ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Mineralocorticoid Receptor (MR). No significant cross-reactivity or interference between Mineralocorticoid Receptor (MR) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.058ng/mL.
  • Intended UseHuman MR ELISA Kit allows for the in vitro quantitative determination of MR , 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 Description
    Principle of the Assay: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mineralocorticoid Receptor (MR). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Mineralocorticoid Receptor (MR). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mineralocorticoid Receptor (MR), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mineralocorticoid Receptor (MR) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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