Human FGF 23 ELISA Kit

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  • Alternative name

    Fibroblast growth factor 23 ELISA KIT; Phosphatonin ELISA KIT; Tumor-derived hypophosphatemia-inducing factorCleaved into the following 2 chains:Fibroblast growth factor 23 N-terminal peptide ELISA KIT; Fibroblast growth factor 23 C-terminal peptideFGF23 ELISA KIT; HYPF ELISA KIT; UNQ3027/PRO9828 ELISA KIT; FGF-23 ELISA KIT

  • Catalog
  • species
  • GeneFGF 23
  • Standard CurveHuman FGF 23 ELISA Kit
  • Other Species Human FGF-23 ELISA KitMouse FGF-23 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of FGF-23. No significant cross-reactivity or interference between FGF-23 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between FGF-23 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 UseHuman FGF 23 ELISA Kit allows for the in vitro quantitative determination of FGF 23 , 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/FamilyCardiovascular
  • Product Description
    Principle of the assay: FGF-23 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for FGF-23. Standards or samples are then added to the microtiter plate wells and FGF-23 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of FGF-23 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for FGF-23 are added to each well to "sandwich" the FGF-23 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 FGF-23 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 FGF-23 concentration in each sample is interpolated from this standard curve.

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