Mouse ES ELISA Kit

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  • Catalog
    E052174
  • species
    Mouse
  • GeneES
  • Standard CurveMouse ES ELISA Kit
  • Other Species Human ES ELISA KitHuman ES-Ab ELISA KitMouse COL18A1/ES ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of ES. No significant cross-reactivity or interference between ES and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between ES 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 pg/mL.
  • Intended UseMouse ES ELISA Kit allows for the in vitro quantitative determination of ES , 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/FamilyMouse ELISA Kit
  • Product Description
    specifical
    Principle of the Assay: ES ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for ES. Standards or samples are then added to the microtiter plate wells and ES if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of ES present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for ES are added to each well to "sandwich" the ES immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain ES and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ES concentration in each sample is interpolated from this standard curve.




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