首页> 外文期刊>Journal of Agricultural and Food Chemistry >RAPID DETECTION OF FUMONISIN B-1 IN CORN-BASED FOOD BY COMPETITIVE DIRECT DIPSTICK ENZYME IMMUNOASSAY ENZYME-LINKED IMMUNOFILTRATION ASSAY WITH INTEGRATED NEGATIVE CONTROL REACTION
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RAPID DETECTION OF FUMONISIN B-1 IN CORN-BASED FOOD BY COMPETITIVE DIRECT DIPSTICK ENZYME IMMUNOASSAY ENZYME-LINKED IMMUNOFILTRATION ASSAY WITH INTEGRATED NEGATIVE CONTROL REACTION

机译:直接直接滴定酶免疫分析法与酶联免疫吸附法联合负控制反应快速检测玉米基食品中的伏马菌素B-1

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摘要

Membrane-based competitive enzyme immunoassays (EIA) in dipstick. and immunofiltration (ELIFA) format for the detection of fumonisin B-1 (FB1) were developed. A nylon membrane was coated with anti-FB1 antibodies and with anti-horseradish peroxidase (HRP) antibodies. A FB1-HRP conjugate was used both as the labeled antigen for competitive assay of FB1 and for noncompetitive binding to the anti-HRP antibodies (negative control). Both tests had visual detection Limits for FB1 in the range of 7.5-10 ng/mL (buffer solutions) and 40-60 ng/g (corn-based food samples). The tests were applied to corn-based food samples, and the results were compared with those of microtiter plate EIA and high-performance Liquid chromatography. With assay times of 60 min (dipsticks) and 10 min (ELIFA), these rapid tests should be useful to qualitatively detect FB1 in corn-based foods.
机译:量油尺中基于膜的竞争性酶免疫法(EIA)。并开发了用于检测伏马菌素B-1(FB1)的免疫过滤(ELIFA)格式。尼龙膜上涂有抗FB1抗体和抗辣根过氧化物酶(HRP)抗体。 FB1-HRP共轭物既用作标记抗原,用于竞争性检测FB1,又用于非竞争性结合抗HRP抗体(阴性对照)。两种测试的FB1视觉检测极限均在7.5-10 ng / mL(缓冲溶液)和40-60 ng / g(基于玉米的食物样品)之间。将测试应用于玉米基食品样品,并将结果与​​微量滴定板EIA和高效液相色谱法进行比较。测定时间分别为60分钟(试纸)和10分钟(ELIFA),这些快速测试对于定性检测玉米食品中的FB1很有用。

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