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  • Alternative name

    Proenkephalin-A ELISA KIT; Opioid growth factor ELISA KIT; OGFPenk ELISA KIT; Penk-rs ELISA KIT; Penk1 ELISA KIT; OGF ELISA KIT

  • Catalog
  • species
  • GeneENK
  • Standard CurveHuman ENK ELISA Kit
  • Other Species Human beta ENK ELISA KitHuman beta-ENK ELISA KitHuman Leu ENK ELISA KitHuman Met ENK ELISA KitMouse b-ENK ELISA KitMouse beta-ENK ELISA KitMouse ENK ELISA KitMouse Leu-ENK ELISA KitMouse Met-ENK ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of ENK. No significant cross-reactivity or interference between ENK and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between ENK 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 UseHuman ENK ELISA Kit allows for the in vitro quantitative determination of ENK , 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/FamilyNeurobiology
  • Product Description
    Princple of the assay: ENK ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for ENK. Standards or samples are then added to the microtiter plate wells and ENK if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of ENK present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for ENK are added to each well to ?sandwich? the ENK 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 ENK 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 ENK concentration in each sample is interpolated from this standard curve.

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