Human MT2 ELISA Kit

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  • Alternative name

    Metallothionein-2 ELISA KIT; Metallothionein-2A ELISA KIT; Metallothionein-II ELISA KIT; MT-IIMT2A ELISA KIT; CES1 ELISA KIT; MT2 ELISA KIT; MT-2 ELISA KIT; MT-II ELISA KIT

  • Catalog
    E024277
  • species
    Human
  • GeneMT2
  • Standard CurveHuman MT2 ELISA Kit
  • Other Species Mouse Mt2 ELISA KitBovine MT2 ELISA KitHamster MT2 ELISA KitMonkey MT2 ELISA KitRat Mt2 ELISA KitSheep MT2 ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1ng/mL.
  • Intended UseHuman MT2 ELISA Kit allows for the in vitro quantitative determination of MT2 , 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/FamilyMicrobiology
  • Product Description
    specifical
    For samples: Serum, plasma, cell culture supernatants, body fluid and tissue homogenate INTENDED USE This MT2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human MT2. This ELISA kit for research use only, not for therapeutic or diagnostic applications! PRINCIPLE OF THE ASSAY MT2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-MT2 antibody and an MT2-HRP conjugate. The assay sample and buffer are incubated together with MT2-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 MT2 concentration since MT2 from samples and MT2-HRP conjugate compete for the anti-MT2 antibody binding site. Since the number of sites is limited, as more sites are occupied by MT2 from the sample, fewer sites are left to bind MT2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The MT2 concentration in each sample is interpolated from this standard curve.


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