Human LDL ELISA Kit

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  • Alternative name

    Low density lipoprotein ELISA KIT; Low density lipoproteinLDLR ELISA KIT;

  • Catalog
    E022955
  • species
    Human
  • GeneLDL
  • Standard CurveHuman LDL ELISA Kit
  • Other Species Human LDL-IC ELISA KitHuman LDL C ELISA KitHuman LDL-C ELISA KitHuman LDL IC ELISA KitMouse LDL-C ELISA KitMouse LDL-IC ELISA KitMouse LDL ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Low Density Lipoprotein (LDL). No significant cross-reactivity or interference between Low Density Lipoprotein (LDL) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.37ng/mL.
  • Intended UseHuman LDL ELISA Kit allows for the in vitro quantitative determination of LDL , 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
    specifical
    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 Low Density Lipoprotein (LDL). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Low Density Lipoprotein (LDL). 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 Low Density Lipoprotein (LDL), 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 Low Density Lipoprotein (LDL) in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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