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GA21转基因玉米实时荧光PCR检测方法的建立 被引量:11

Establishment of the Real |time Fluorescent PCR Detection Method for Genetically Modified GA21 Maize
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摘要 成功建立了实时荧光PCR鉴定检测转基因玉米GA2 1品系的方法。该方法通过GA2 1玉米品系的OTP mEPSPS边界的 2 70bp和 1 33bp靶序列 ,设计品系特异性检测引物和探针 ,同时针对Pactin 1 mEPSPS边界的 430bp靶序列设计品系特异性检测引物 ,应用实时荧光PCR和PCR技术 ,特异性检测GA2 1玉米品系。结果表明 ,应用实时荧光PCR的TaqMan探针技术检测转基因作物边界序列 ,不仅可以达到品系鉴定的目的 ,而且该方法和常规PCR比特异性强 ,简便快速 ,同时实验采用完全闭管检测 ,又降低了污染机会 ,为转基因作物的品系鉴定检测提供了新方法。 A event-specific real-time fluorescent PCR (RTF PCR) method was established for detection and identification of the genetically modified GA21 maize.The PCR primers and TaqMan probes were designed based on the GA21 border sequence of 270bp and 133bp of OTP/mEPSPS and 430bp of P actin 1/mEPSPS.The results show that the TaqMan probe could detect and identify GA21 maize specifically.RTF PCR method is much convenient and quicker to operate than common PCR,much less contamination will occur because whole detection process is finished in the contained tubes.RTF PCR could be a new method for detection of genetically modified organism event-specifically. ;
出处 《中国生物工程杂志》 CAS CSCD 2003年第8期87-91,95,共6页 China Biotechnology
基金 国家转基因植物研究与产业化专项课题 (JOO- C- 0 0 5 ) 国家标准研制项目 (B2 0 2 - 2 0 0 1)
关键词 GA21转基因玉米 实时荧光PCR 检测 品系 检测引物 PCR Real-time fluorescent PCR GA21 GM-maize Detection and identification
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参考文献11

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