Human Efabp5 ELISA Kit

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  • Alternative name

    Fatty acid-binding protein, epidermal ELISA KIT; Cutaneous fatty acid-binding protein ELISA KIT; C-FABP ELISA KIT; DA11 ELISA KIT; Epidermal-type fatty acid-binding protein ELISA KIT; E-FABP ELISA KIT; Fatty acid-binding protein 5Fabp5 ELISA KIT; C-FABP ELISA KIT; E-FABP ELISA KIT

  • Catalog
  • species
  • GeneEfabp5
  • Standard CurveHuman Efabp5 ELISA Kit
  • Other Species Mouse Efabp5 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of EFABP5. No significant cross-reactivity or interference between EFABP5 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between EFABP5 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 Efabp5 ELISA Kit allows for the in vitro quantitative determination of Efabp5 , 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/FamilyMetabolism
  • Product Description
    Intended Uses: This EFABP5 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human EFABP5. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: EFABP5 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for EFABP5. Standards or samples are then added to the microtiter plate wells and EFABP5 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of EFABP5 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for EFABP5 are added to each well to "sandwich" the EFABP5 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 EFABP5 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 EFABP5 concentration in each sample is interpolated from this standard curve.

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