摘要
报导一种赤潮甲藻单个细胞DNA的制备方法.该法仅需1或数个甲藻细胞,在常规实验条件下,20~30min即可完成整个过程.此方法的建立,可直接对自然种群进行分子分析,避免了实验室培养种与自然种群的差异,同时,使材料的来源并不依赖于甲藻培养技术的完善.最后。
A method for PCR amplification of Dionoflagellate rDNA with individual cells was reported and its applification for the identification of “red tide” algae species was discussed. It was demonstrated that the single cell PCR method was useful in analysing natural populations.This method eliminated the differences between lab investigation and natural population, and solved the problems resulting from the analysis of rRNA gene for those organisms which is difficult or even impossible to propagate in the lab.
出处
《中山大学学报(自然科学版)》
CAS
CSCD
北大核心
1997年第4期66-69,共4页
Acta Scientiarum Naturalium Universitatis Sunyatseni
基金
博士后日常经费资助
关键词
甲藻
DPS系统
微量
DNA制备
分子鉴定
赤潮
藻类
dinoflagellate, DPS system, preparation of trace DNA, molecular identification