摘要
运用常规 PCR方法和实时荧光 PCR方法对转基因抗虫保铃棉外源基因 Ca MV 35 S启动子、NOS终止子、标记基因NPT II和目的基因 Cry IA(c)进行了检测。建立了快速、准确的抗虫保铃棉籽转基因成分的 PCR检测方法。
The exogenous CaMV 35S promoter, NOS terminator, NPT II and CryIA(c) gene in genetically modified Bollgard cotton were detected by conventional PCR and real time PCR, so the accurate and fast PCR detection methods were conducted.
出处
《种子》
CSCD
北大核心
2003年第5期38-40,共3页
Seed