摘要
采用黄化苗,按氯仿—异戊醇—RNA酶法获得DNA粗制品,后经酚—氯仿—乙戊醇纯化得12种作物新品种的PCR反应模板DNA。结果测量获得的数据和曲线表明:采用本实验的提取方法,可得到具有一定纯度和数量的DNA,完全可以满足PCR反应所需。
Crude DNA can be obtained from yellowing seedling with chlorom RNAase. After purification and extraction of phenol chloroform ethanol, the seed PCR template DNA twelve crops have been gained. Data and figures show that DNA with certain purity and quantity could be recovered, sufficient for Polymerase Chain Reaction(PCR).
出处
《西北大学学报(自然科学版)》
CAS
CSCD
北大核心
1998年第1期64-67,共4页
Journal of Northwest University(Natural Science Edition)