摘要
建立了以菌落PCR产物作为DNA测序模板进行快速测序的技术方法。研究结果表明,采用菌落PCR技术,以载体插入位点两端序列互补的通用引物(如M13正反向引物)为引物,在控制菌落PCR反应条件的情况下,不仅可用于筛选和鉴定阳性克隆,而且菌落PCR产物还可作为DNA测序模板,结果准确可靠。与常规质粒测序方法比较,该法快速、简便,但对具有PolyT、PolyA过多的序列进行测序时,该法测序效率较低。
A method for direct sequencing using colony PCR products was established. Under controlled conditions, colony PCR could be used to screen and identify positive clone, and its products could be used as sequencing templates directly. The sequencing result was reliable. Compared with conventional plasmid DNA sequencing method, colony PCR products sequencing method was faster and simpler. However, when the products were used to sequence the DNA with long PolyT and PolyA, the sequencing efficiency was low.
出处
《中国水稻科学》
CAS
CSCD
北大核心
2005年第5期463-466,共4页
Chinese Journal of Rice Science
基金
浙江省分析测试基金资助项目(04185)
