Mouse ACA-IgM ELISA Kit

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  • Catalog
    E042374
  • species
    Mouse
  • GeneACA-IgM
  • Other Species Human ACA-IgM ELISA KitHuman ACA IgM ELISA KitHuman ACA (IgM) ELISA Kit
  • SpecificityThis kit recognizes natural and recombinant Mouse ACA-IgM. No significant cross-reactivity or interference between Mouse ACA-IgM and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of Mouse ACA-IgM is 1.875ng/mL (The sensitivity of this assay or lowest detectable limit (LDL) was defined as the lowest protein concentration that could be differentiated from zero.)
  • Intended UseMouse ACA-IgM ELISA Kit allows for the in vitro quantitative determination of ACA-IgM , 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: This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antigen specific to ACA-IgM. Standards or samples are added to the appropriate micro ELISA plate wells and combined with the specific antigen. Then a biotinylated detection antigen specific for ACA-IgM and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain ACA-IgM, biotinylated detection antigen and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of ACA-IgM.You can calculate the concentration of ACA-IgM in the samples by comparing the OD of the samples to the standard curve.



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