摘要
芝麻是重要的食品过敏原之一,微小剂量即可引起严重的过敏反应。针对芝麻过敏蛋白-2S白蛋白的基因序列设计PCR扩增引物,建立并优化芝麻过敏原检测的普通聚合酶链式反应(PCR)和实时荧光定量聚合酶链式反应(Real-time PCR)方法。结果表明,两种方法的最低检测限分别为0.1,0.01ng DNA,该方法特异性良好,成本较低,具有一定的应用价值。
Sesame is an important food allergen;low-level doses can cause severe allergic reactions.In this paper,PCR primers were designed based on sesame allergy protein(2S albumin) gene sequence,and conventional PCR and Real-time PCR were established and optimized.The lowest DNA content that can be detected for conventional PCR was 0.1 ng and 0.01 ng for real-time PCR,respectively.The specificity of the methods is good and can be widely used.
出处
《食品与机械》
CSCD
北大核心
2012年第2期52-55,65,共5页
Food and Machinery