Human F8 Ag ELISA Kit

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  • Alternative name

    Coagulation factor VIII ELISA KIT; Antihemophilic factor ELISA KIT; AHF ELISA KIT; Procoagulant componentCleaved into the following 4 chains:Factor VIIIa heavy chain, 200 kDa isoform ELISA KIT; Factor VIIIa heavy chain, 92 kDa isoform ELISA KIT; Factor VIII B chain ELISA KIT; Factor VIIIa light chainF8 ELISA KIT; F8C ELISA KIT; AHF ELISA KIT

  • Catalog
    E009836
  • species
    Human
  • GeneF8 Ag
  • Standard CurveHuman F8 Ag ELISA Kit
  • Other Species Human F8-AG ELISA KitMouse F8-Ag ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of FVIII-Ag. No significant cross-reactivity or interference between FVIII-Ag and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between FVIII-Ag 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 F8 Ag ELISA Kit allows for the in vitro quantitative determination of F8 Ag , 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: FVIII-Ag ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-FVIII-Ag antibody and an FVIII-Ag-HRP conjugate. The assay sample and buffer are incubated together with FVIII-Ag-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 FVIII-Ag concentration since FVIII-Ag from samples and FVIII-Ag-HRP conjugate compete for the anti-FVIII-Ag antibody binding site. Since the number of sites is limited, as more sites are occupied by FVIII-Ag from the sample, fewer sites are left to bind FVIII-Ag-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The FVIII-Ag concentration in each sample is interpolated from this standard curve.



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