Mouse nNOS ELISA Kit

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  • Alternative name

    Nitric oxide synthase, brain ELISA KIT; Constitutive NOS ELISA KIT; NC-NOS ELISA KIT; NOS type I ELISA KIT; Neuronal NOS ELISA KIT; N-NOS ELISA KIT; nNOS ELISA KIT; Peptidyl-cysteine S-nitrosylase NOS1 ELISA KIT; bNOSNOS1 ELISA KIT; N-NOS ELISA KIT; nNOS ELISA KIT

  • Catalog
  • species
  • GenenNOS
  • Standard CurveMouse nNOS ELISA Kit
  • Other Species Human nNOS ELISA KitHuman NOS1/nNOS ELISA KitMouse NOS1/nNOS ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of nNOS. No significant cross-reactivity or interference between nNOS and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between nNOS and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseMouse nNOS ELISA Kit allows for the in vitro quantitative determination of nNOS , 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
    Intended Uses||This nNOS ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse nNOS. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: nNOS ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-nNOS antibody and an nNOS-HRP conjugate. The assay sample and buffer are incubated together with nNOS-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the nNOS concentration since nNOS from samples and nNOS-HRP conjugate compete for the anti-nNOS antibody binding site. Since the number of sites is limited, as more sites are occupied by nNOS from the sample, fewer sites are left to bind nNOS-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The nNOS concentration in each sample is interpolated from this standard curve.

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