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Plant Phosphatidic acid ELISA kit
INTENDED USEThe PA ELISA is to be used for the quantitative determination of PA. The assay will recognize both natural and recombinant PA. The kit has been configured for research use only and is not to be used in diagnostic procedures.PRINCIPLE OF THE METHODThe PA kit is a solid phase phase sandwich enzyme linked immuno sorbent assay（ELISA）. Samples , including standards of known PA concentrations and unknowns are pipetted into these wells. During the first incubation, the PAantigen and a biotinylated monoclonal antibody specific for PAare simultaneously incubated. After washing, the enzyme（streptavidin-peroxydase）is added. After incubation and washing to remove all the unbound enzyme, a substrate solution which is acting on the bound enzyme is added to induce a coloured reaction product. The intensity of this coloured product is directly proportional to the concentration of PApresent in the samples.REAGENTS PROVIDED AND RECONSTTTUTIONREAGENTS（Store at 2-8℃）1×96 WELLS0.5×96 WELLSRECONSTTTUTION96/48-wells microtiter plates10.5Ready-to-usePlastiv cover21Ready-to-useStandard: 40ng/ml1Vials （0.6ml）0.5Vials （0.3ml）See reagents preparation on page 3Blank control1Vials （1.0ml）1Vials （0.5ml）Ready-to-useStandard Diluent1Vials （5ml）1Vials （2.5ml）Ready-to-useBiotinylated anti-PA1Vials （6ml）1Vials （3.0ml）Ready-to-useStreptavidin-HRP1Vials （10ml）1Vials （5.0ml）Ready-to-useWashing Buffer1Vials （60ml）1Vials （30ml）20× concentrateSubstrate A1Vials （6.0ml）1Vials （3.0ml）Ready-to-useSubstrate B1Vials 6.0ml）1Vials （3.0ml）Ready-to-useStopping Solution1Vials （6.0ml）1Vials （3.0ml）Ready-to-useMATERIAL REQUIRED BUT NOT PROVIDEDl Distilled waterl Pipettes:10ul、50ul、100ul、200ul、1000ul。l Vortex mixer and magnetic stirrer.INTENDED USEThe PA ELISA is to be used for the quantitative determination of PA. The assay will recognize both natural and recombinant PA. The kit has been configured for research use only and is not to be used in diagnostic procedures.PRINCIPLE OF THE METHODThe PA kit is a solid phase phase sandwich enzyme linked immuno sorbent assay（ELISA）. Samples , including standards of known PA concentrations and unknowns are pipetted into these wells. During the first incubation, the PAantigen and a biotinylated monoclonal antibody specific for PAare simultaneously incubated. After washing, the enzyme（streptavidin-peroxydase）is added. After incubation and washing to remove all the unbound enzyme, a substrate solution which is acting on the bound enzyme is added to induce a coloured reaction product. The intensity of this coloured product is directly proportional to the concentration of PApresent in the samples.REAGENTS PROVIDED AND RECONSTTTUTIONREAGENTS（Store at 2-8℃）1×96 WELLS0.5×96 WELLSRECONSTTTUTION96/48-wells microtiter plates10.5Ready-to-usePlastiv cover21Ready-to-useStandard: 40ng/ml1Vials （0.6ml）0.5Vials （0.3ml）See reagents preparation on page 3Blank control1Vials （1.0ml）1Vials （0.5ml）Ready-to-useStandard Diluent1Vials （5ml）1Vials （2.5ml）Ready-to-useBiotinylated anti-PA1Vials （6ml）1Vials （3.0ml）Ready-to-useStreptavidin-HRP1Vials （10ml）1Vials （5.0ml）Ready-to-useWashing Buffer1Vials （60ml）1Vials （30ml）20× concentrateSubstrate A1Vials （6.0ml）1Vials （3.0ml）Ready-to-useSubstrate B1Vials 6.0ml）1Vials （3.0ml）Ready-to-useStopping Solution1Vials （6.0ml）1Vials （3.0ml）Ready-to-useMATERIAL REQUIRED BUT NOT PROVIDEDl Distilled waterl Pipettes:10ul、50ul、100ul、200ul、1000ul。l Vortex mixer and magnetic stirrer.