双重实时荧光PCR法测定食品中大豆、小麦过敏原

被引:4
作者
金萍
丁洪流
张敏
金晓红
机构
[1] 苏州市产品质量监督检验院
关键词
实时荧光聚合酶链反应; 食品过敏原; 大豆; 小麦;
D O I
10.13652/j.spjx.1003.5788.2022.90116
中图分类号
TS207.3 [食品分析与检验];
学科分类号
摘要
目的:为食品监管部门有效检测食品中大豆、小麦过敏原提供技术支撑。方法:分别依据小麦醇溶蛋白基因及大豆Lectin基因为模板设计并创建TaqMan探针双重荧光PCR方法,大豆Lectin基因检测采用FAM标记,小麦醇溶蛋白基因检测采用HEX标记,同时以真核生物18S rRNA作为内参基因确保检测体系的有效性。结果:所创建的实时多重TaqMan探针PCR体系对大豆、小麦过敏原之外的物种成分无荧光扩增;大豆、小麦混合样品的检出限均能达到0.01%(质量分数)。结论:所创建的实时多重TaqMan探针PCR体系针对大豆、小麦过敏原有高特异性,可用于食品中过敏原大豆、小麦成分的同步快速检测。
引用
收藏
页码:59 / 63+102 +102
页数:6
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