Human Lp PL A2 ELISA Kit

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  • Alternative name

    Platelet-activating factor acetylhydrolase ELISA KIT; 1-alkyl-2-acetylglycerophosphocholine esterase ELISA KIT; 2-acetyl-1-alkylglycerophosphocholine esterase ELISA KIT; Group-VIIA phospholipase A2 ELISA KIT; gVIIA-PLA2 ELISA KIT; LDL-associated phospholipase A2 ELISA KIT; LDL-PLA(2) ELISA KIT; PAF 2-acylhydrolasePLA2G7 ELISA KIT; PAFAH ELISA KIT; PAF acetylhydrolase ELISA KIT; gVIIA-PLA2 ELISA KIT; LDL-PLA(2) ELISA KIT

  • Catalog
    E022863
  • species
    Human
  • GeneLp PL A2
  • Standard CurveHuman Lp PL A2 ELISA Kit
  • Other Species Human Lp-PL-A2 ELISA KitMouse Lp-PL-A2 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Lp-PLA2. No significant cross-reactivity or interference between Lp-PLA2 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between Lp-PLA2 and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseHuman Lp PL A2 ELISA Kit allows for the in vitro quantitative determination of Lp PL A2 , 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
    specifical
    Intended Uses: This Lp-PLA2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human Lp-PLA2. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay||Lp-PLA2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-Lp-PLA2 antibody and an Lp-PLA2-HRP conjugate. The assay sample and buffer are incubated together with Lp-PLA2-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the Lp-PLA2 concentration since Lp-PLA2 from samples and Lp-PLA2-HRP conjugate compete for the anti-Lp-PLA2 antibody binding site. Since the number of sites is limited, as more sites are occupied by Lp-PLA2 from the sample, fewer sites are left to bind Lp-PLA2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The Lp-PLA2 concentration in each sample is interpolated from this standard curve.



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