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        大麻素(AEA)酶聯(lián)免疫吸附檢測試劑盒
        ELK8269
        規(guī)格: 價(jià)格:
        48T ¥2240.00
        96T ¥3200.00

        Overview 文獻(xiàn)

        Product name: AEA(Anandamide) ELISA Kit
        Reactivity: General
        Alternative Names: N-Arachidonoylethanolamine
        Assay Type: Competitive Inhibition
        Sensitivity: 0.94 ng/mL
        Standard: 200 ng/mL
        Detection Range: 3.13-200 ng/mL
        Sample Type: serum, plasma and other biological fluids
        Assay Length: 2h
        Research Area: Neuro science; Immunity
        Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with AEA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to AEA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 AEA in the samples is then determined by comparing the OD of the samples to the standard curve.

        標(biāo)準(zhǔn)曲線

        Concentration (ng/mL) OD Corrected OD
        200.00 0.199
        100.00 0.385
        50.00 0.621
        25.00 0.998
        12.50 1.253
        6.25 1.522
        3.13 1.786
        0.00 2.375

        精密度

        Intra-assay Precision (Precision within an assay):CV%<8%

        Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

        Inter-assay Precision (Precision between assays):CV%<10%

        Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.

        回收率

        Matrices listed below were spiked with certain level of recombinant AEA and the recovery rates were calculated by comparing the measured value to the expected amount of AEA in samples.
        Matrix Recovery range Average
        serum(n=5) 80-95% 87%
        EDTA plasma(n=5) 85-97% 91%
        Heparin plasma(n=5) 92-107% 101%

        線性

        The linearity of the kit was assayed by testing samples spiked with appropriate concentration of AEA and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
        Matrix 1:2 1:4 1:8 1:16
        serum(n=5) 95-103% 86-92% 86-92% 89-97%
        EDTA plasma(n=5) 95-104% 82-96% 92-105% 83-92%
        Heparin plasma(n=5) 79-94% 96-105% 87-101% 82-90%
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