One-step isolation of plant DNA suitable for PCR amplification

被引:17
作者
Burr, K
Harper, R
Linacre, A
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, Forens Sci Unit, Glasgow G1 1XW, Lanark, Scotland
[2] Univ Leicester, MRC, Toxicol Unit, Leicester LE1 7RH, Leics, England
[3] Florida Int Univ, Int Forens Res Inst, Miami, FL 33199 USA
关键词
chloroplast markers; DNA isolation; grasses; RAPD;
D O I
10.1007/BF02772835
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report a one-step extraction technique for the isolation of plant DNA. DNA suitable for amplification by PCR can be produced from leaf material smaller than 0.3 mm(2) in less than 20 min, with no tube changes. The method was tested on several plant species. The described method was found to extract DNA that could be amplified without any further purification or treatment. The isolated DNA was amplified using a universal chloroplast primer set. The method was validated by comparing size of PCR products generated by the novel method to PCR products generated using standard DNA isolation techniques.
引用
收藏
页码:367 / 371
页数:5
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