Mouse LA ELISA Kit

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  • Alternative name

    Lactic acid dehydrogenase ELISA KIT; Lactic acid dehydrogenase

  • Catalog
  • species
  • GeneLA
  • Standard CurveMouse LA ELISA Kit
  • Other Species Human alpha-La ELISA KitHuman D La ELISA KitHuman D-LA ELISA KitHuman LA ELISA KitHuman LA DR ELISA KitHuman LAC/LA ELISA KitHuman SS B/La ELISA KitHuman SS-B/La ELISA KitMouse alpha-La ELISA KitMouse D-LA ELISA KitMouse LA-DR ELISA KitMouse LAC/LA ELISA KitMouse SS-B/La ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1mmol/L.
  • Intended UseMouse LA ELISA Kit allows for the in vitro quantitative determination of LA , 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
    Principle of the Assay: LA ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for LA. Standards or samples are then added to the microtiter plate wells and LA if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of LA present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for LA are added to each well to "sandwich" the LA 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 LA 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 LA concentration in each sample is interpolated from this standard curve.

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