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  • Alternative name

    Cytochrome b-c1 complex subunit 1, mitochondrial ELISA KIT; Complex III subunit 1 ELISA KIT; Core protein I ELISA KIT; Ubiquinol-cytochrome-c reductase complex core protein 1UQCRC1 ELISA KIT;

  • Catalog
  • species
  • GeneUQCR
  • Standard CurveHuman UQCR ELISA Kit
  • Other Species Mouse UQCR ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Ubiquinol Cytochrome C Reductase (UQCR). No significant cross-reactivity or interference between Ubiquinol Cytochrome C Reductase (UQCR) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.27ng/mL.
  • Intended UseHuman UQCR ELISA Kit allows for the in vitro quantitative determination of UQCR , 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 Ubiquinol Cytochrome C Reductase (UQCR). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Ubiquinol Cytochrome C Reductase (UQCR). 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 Ubiquinol Cytochrome C Reductase (UQCR), 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 Ubiquinol Cytochrome C Reductase (UQCR) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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