Human DUB ELISA Kit

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  • Alternative name

    Ubiquitin carboxyl-terminal hydrolase 15 ELISA KIT; Deubiquitinating enzyme 15 ELISA KIT; Ubiquitin thioesterase 15 ELISA KIT; Ubiquitin-specific-processing protease 15 ELISA KIT; Unph-2 ELISA KIT; Unph4USP15 ELISA KIT; KIAA0529 ELISA KIT

  • Catalog
    E011807
  • species
    Human
  • GeneDUB
  • Standard CurveHuman DUB ELISA Kit
  • Other Species Mouse DUB ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of DUB. No significant cross-reactivity or interference between DUB and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between DUB 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 DUB ELISA Kit allows for the in vitro quantitative determination of DUB , 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: DUB ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-DUB antibody and an DUB-HRP conjugate. The assay sample and buffer are incubated together with DUB-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 DUB concentration since DUB from samples and DUB-HRP conjugate compete for the anti-DUB antibody binding site. Since the number of sites is limited, as more sites are occupied by DUB from the sample, fewer sites are left to bind DUB-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The DUB concentration in each sample is interpolated from this standard curve.



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