Human AT ELISA Kit

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  • Alternative name

    Antithrombin-III ELISA KIT; Serpin C1SERPINC1 ELISA KIT; AT3 ELISA KIT; ATIII ELISA KIT

  • Catalog
    E003140
  • species
    Human
  • GeneAT
  • Standard CurveHuman AT ELISA Kit
  • Other Species Human alpha1-AT ELISA KitHuman AT-1 ELISA KitHuman AT III ELISA KitHuman AT-III ELISA KitHuman Anti-AT-III ELISA KitMouse alpha1-AT ELISA KitMouse AT-1 ELISA KitMouse AT II RI ELISA KitMouse AT ELISA KitMouse AT-III ELISA KitHuman ANG II R1-Ab ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Antithrombin (AT). No significant cross-reactivity or interference between Antithrombin (AT) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 1.38ng/mL.
  • Intended UseHuman AT ELISA Kit allows for the in vitro quantitative determination of AT , 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 Antithrombin (AT). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Antithrombin (AT). 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 Antithrombin (AT), 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 Antithrombin (AT) in the samples is then determined by comparing the O.D. of the samples to the standard curve.




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