摘要
介绍在PCR检测体系中一种快速提取病毒DNA的方法。利用高盐缓冲液溶液释放病毒DNA,同时利用葡聚糖凝胶微柱纯化提取液,有效消除样品中PCR抑制物质并直接作为PCR反应模板扩增检测病毒。该法无需任何特殊设备,适合对大量植株进行大通量的检测分析。
A rapid plant tissue preparation protocol suitable for the detection of DNA viruses by the polymerase chain reaction (PCR) was described. Liberation of viruses from leaves in an appropriate buffer and high salt may allow sufficient template release for direct use in PCR. Single-use Sephadex gel columns provide excellent purification of crude sap which can reduce plant inhibitory factors which may interfer with PCR and introduced the extracted sap directly into PCR reaction mixture.
出处
《生物技术通讯》
CAS
2005年第5期533-534,共2页
Letters in Biotechnology
基金
科技部农业微生物资源平台项目(2004DKA30560-8)
农业部南亚热带作物专项(2004LY07)
中国热带农业科学院重点研究资助方向