Human MIg ELISA Kit

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  • Alternative name

    C-X-C motif chemokine 9 ELISA KIT; Small-inducible cytokine B9CXCL9 ELISA KIT;

  • Catalog
    E024892
  • species
    Human
  • GeneMIg
  • Standard CurveHuman MIg ELISA Kit
  • Other Species Human MIG/CXCL9 ELISA KitMouse MIg ELISA KitMouse CXCL9/MIG ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Monokine Induced By Interferon Gamma (MIg). No significant cross-reactivity or interference between Monokine Induced By Interferon Gamma (MIg) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 13.1pg/mL.
  • Intended UseHuman MIg ELISA Kit allows for the in vitro quantitative determination of MIg , 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: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Monokine Induced By Interferon Gamma (MIg). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Monokine Induced By Interferon Gamma (MIg). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Monokine Induced By Interferon Gamma (MIg), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Monokine Induced By Interferon Gamma (MIg) in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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