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Mouse ERa ELISA Kit

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  • Alternative name

    Estrogen receptor ELISA KIT; ER-alpha ELISA KIT; Estradiol receptor ELISA KIT; Nuclear receptor subfamily 3 group A member 1ESR1 ELISA KIT; ESR ELISA KIT; NR3A1 ELISA KIT; ER ELISA KIT
  • Catalog
    E052155
  • species
    Mouse
  • GeneERa
  • Standard CurveMouse ERa ELISA Kit
  • Other Species Human ERa ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Estrogen Receptor Alpha (ERa). No significant cross-reactivity or interference between Estrogen Receptor Alpha (ERa) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.146ng/mL.
  • Intended UseMouse ERa ELISA Kit allows for the in vitro quantitative determination of ERa , 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
    specifical    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 Estrogen Receptor Alpha (ERa). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Estrogen Receptor Alpha (ERa). 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 Estrogen Receptor Alpha (ERa), 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 Estrogen Receptor Alpha (ERa) in the samples is then determined by comparing the O.D. of the samples to the standard curve.


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