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  • Alternative name

    Perilipin-2 ELISA KIT; Adipophilin ELISA KIT; Adipose differentiation-related protein ELISA KIT; ADRPPlin2 ELISA KIT; Adfp ELISA KIT; Adrp ELISA KIT; ADRP ELISA KIT

  • Catalog
  • species
  • GeneADRP
  • Standard CurveHuman ADRP ELISA Kit
  • Other Species Mouse ADRP ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Adipose Differentiation Related Protein (ADRP). No significant cross-reactivity or interference between Adipose Differentiation Related Protein (ADRP) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.055ng/mL.
  • Intended UseHuman ADRP ELISA Kit allows for the in vitro quantitative determination of ADRP , 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
    Principle of the Assay: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Adipose Differentiation Related Protein (ADRP). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Adipose Differentiation Related Protein (ADRP). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Adipose Differentiation Related Protein (ADRP), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Adipose Differentiation Related Protein (ADRP) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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