Human MT ND1 ELISA Kit

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  • Alternative name

    NADH-ubiquinone oxidoreductase chain 1 ELISA KIT; NADH dehydrogenase subunit 1MT-ND1 ELISA KIT; MTND1 ELISA KIT; NADH1 ELISA KIT; ND1 ELISA KIT

  • Catalog
    E025806
  • species
    Human
  • GeneMT ND1
  • Standard CurveHuman MT ND1 ELISA Kit
  • Other Species Mouse MT-ND1 ELISA KitBovine MT-ND1 ELISA KitCanine MT-ND1 ELISA KitChicken MT-ND1 ELISA KitHorse MT-ND1 ELISA KitHuman MT-ND1 ELISA KitPorcine MT-ND1 ELISA KitRabbit MT-ND1 ELISA KitSheep MT-ND1 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of MT ND1. No significant cross-reactivity or interference between MT ND1 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between MT ND1 and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseHuman MT ND1 ELISA Kit allows for the in vitro quantitative determination of MT ND1 , 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: MT ND1 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-MT ND1 antibody and an MT ND1-HRP conjugate. The assay sample and buffer are incubated together with MT ND1-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the MT ND1 concentration since MT ND1 from samples and MT ND1-HRP conjugate compete for the anti-MT ND1 antibody binding site. Since the number of sites is limited, as more sites are occupied by MT ND1 from the sample, fewer sites are left to bind MT ND1-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The MT ND1 concentration in each sample is interpolated from this standard curve.




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