Human GAD67 ELISA Kit

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  • Alternative name

    Glutamate decarboxylase 1 ELISA KIT; 67 kDa glutamic acid decarboxylase ELISA KIT; GAD-67 ELISA KIT; Glutamate decarboxylase 67 kDa isoformGAD1 ELISA KIT; GAD ELISA KIT; GAD67 ELISA KIT; GAD-67 ELISA KIT

  • Catalog
    E002591
  • species
    Human
  • GeneGAD67
  • Standard CurveHuman GAD67 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of GAD67-Ab. No significant cross-reactivity or interference between GAD67-Ab and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between GAD67-Ab and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 ng/mL.
  • Intended UseHuman GAD67 ELISA Kit allows for the in vitro quantitative determination of GAD67 , 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/FamilyImmunology
  • Product Description
    specifical
    Principle of the assay: GAD67-Ab ELISA kit applies the competitive enzyme immunoassay technique utilizing GAD67 antigen and an GAD67-Ab-HRP conjugate. The assay sample and buffer are incubated together with GAD67-Ab-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 GAD67-Ab concentration since GAD67-Ab from samples and GAD67-Ab-HRP conjugate compete for the GAD67 antigen binding site. Since the number of sites is limited, as more sites are occupied by GAD67-Ab from the sample, fewer sites are left to bind GAD67-Ab-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The GAD67-Ab concentration in each sample is interpolated from this standard curve.




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