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Human GM1b ELISA Kit

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  • Catalog
    E002578
  • species
    Human
  • GeneGM1b
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Anti-GM1b. No significant cross-reactivity or interference between Anti-GM1b and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between Anti-GM1b 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 GM1b ELISA Kit allows for the in vitro quantitative determination of GM1b , 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/FamilyCell Biology
  • Product Description
    specifical
    Intended Uses: This Anti-GM1b ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human Anti-GM1b. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay||Anti-GM1b ELISA kit applies the competitive enzyme immunoassay technique utilizing Ganglioside M1b antigen and an Anti-GM1b-HRP conjugate. The assay sample and buffer are incubated together with Anti-GM1b-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 Anti-GM1b concentration since Anti-GM1b from samples and Anti-GM1b-HRP conjugate compete for the Ganglioside M1b antigen binding site. Since the number of sites is limited, as more sites are occupied by Anti-GM1b from the sample, fewer sites are left to bind Anti-GM1b-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The Anti-GM1b concentration in each sample is interpolated from this standard curve.


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