Human aFGF ELISA Kit

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  • Alternative name

    Fibroblast growth factor 1 ELISA KIT; Acidic fibroblast growth factor ELISA KIT; aFGF ELISA KIT; Endothelial cell growth factor ELISA KIT; ECGF ELISA KIT; Heparin-binding growth factor 1 ELISA KIT; HBGF-1FGF1 ELISA KIT; FGFA ELISA KIT; FGF-1 ELISA KIT; aFGF ELISA KIT; ECGF ELISA KIT; HBGF-1 ELISA KIT

  • Catalog
  • species
  • GeneaFGF
  • Standard CurveHuman aFGF ELISA Kit
  • Other Species Human aFGF/FGF-1 ELISA KitHuman AFGF-1 ELISA KitHuman AFGF 1 ELISA KitHuman AFGF/FGF1 ELISA KitMouse aFGF ELISA KitMouse AFGF-1 ELISA KitMouse AFGF/FGF1 ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 pg/mL.
  • Intended UseHuman aFGF ELISA Kit allows for the in vitro quantitative determination of aFGF , 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/FamilyCancer
  • Product Description
    Principle of the Assay: AFGF ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for AFGF. Standards or samples are then added to the microtiter plate wells and AFGF if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of AFGF present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for AFGF are added to each well to "sandwich" the AFGF 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 AFGF 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 AFGF concentration in each sample is interpolated from this standard curve.

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