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食品研究与开发:2021,42(3):146-150
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酶联免疫吸附法快速检测黄曲霉毒素
(1.天津农学院食品科学与生物工程学院,天津 300384;2.天津市农副产品深加工技术工程中心,天津 300384)
Rapid Detection of Aflatoxin by Enzyme-linked Immunosorbent Assay
(1.Department of Food Science and Biology Engineering,Tianjin Agricultural University,Tianjin 300384,China;2.Tianjin Agricultural and Sideline Products Engineering Center of Deep Processing Technology,Tianjin 300384,China)
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投稿时间:2020-06-28    
中文摘要: 结合间接竞争反应机制,运用酶联免疫吸附技术(enzyme-linked immunosorbent assay,ELISA),从抗原(antigen,Ag)包被时间、体系反应温度、酶标二抗作用时间、显色时间等主要因素开展快速检测黄曲霉毒素改进方法的研究。研究结果表明适宜的优化条件为:采用Ag包被20 h、反应温度24℃左右、酶标二抗作用时间30 min、底物显色时间15min。通过对饲料等11种样本的检测得出:半抑制浓度IC50<0.1μg/L,添加回收率在67%~116%,灵敏度达到0.03 μg/L,线性系数>0.99,板内变异小于5%。检测试验结果良好,表明该改进方法具有可行性。
Abstract:Combined with indirect competitive response mechanism,enzyme-linked immunosorbent assay(ELISA)was used to study improved methods for rapid detection of aflatoxin from main factors of antigen(Ag)including duration of inclusion,systemic reaction temperature,time of enzyme-linked immunosorbent assay,color development time,etc.The results showed that the optimal conditions were as follows:Ag coating was used for 20 h,the reaction temperature was around 24℃,the reaction time was 30 min,and the substrate chromogenic time was 15 min.Through the detection of 11 kinds of samples,such as feed,it could be concluded that the semi-inhibitory concentration IC50was less than 0.1 μg/L,the recovery rate was 67 %-116 %,the sensitivity and effective detection were 0.03 μg/L,the linear coefficient was greater than 0.99,and the in-board variation was less than 5 %.The good test results showed that the improved method was feasible.
文章编号:202103024     中图分类号:    文献标志码:
基金项目:天津市科技计划项目(14ZCZDNC00003)
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