Mouse Nav1.7 ELISA Kit

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  • Alternative name

    Sodium channel protein type 9 subunit alpha ELISA KIT; Neuroendocrine sodium channel ELISA KIT; hNE-Na ELISA KIT; Peripheral sodium channel 1 ELISA KIT; PN1 ELISA KIT; Sodium channel protein type IX subunit alpha ELISA KIT; Voltage-gated sodium channel subunit alpha Nav1.7SCN9A ELISA KIT; NENA ELISA KIT; hNE-Na ELISA KIT; PN1 ELISA KIT

  • Catalog
  • species
  • GeneNav1.7
  • Other Species Human Nav1.7 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of NAV1.7. No significant cross-reactivity or interference between NAV1.7 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between NAV1.7 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 Nav1.7 ELISA Kit allows for the in vitro quantitative determination of Nav1.7 , 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 NAV1.7 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse NAV1.7. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: NAV1.7 ELISA kit applies the competitive enzyme immunoassay technique utilizing a Polyclonal anti-NAV1.7 antibody and an NAV1.7-HRP conjugate. The assay sample and buffer are incubated together with NAV1.7-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 NAV1.7 concentration since NAV1.7 from samples and NAV1.7-HRP conjugate compete for the anti-NAV1.7 antibody binding site. Since the number of sites is limited, as more sites are occupied by NAV1.7 from the sample, fewer sites are left to bind NAV1.7-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The NAV1.7 concentration in each sample is interpolated from this standard curve.

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