HIGH-SPEED PARALLEL SEPARATION OF DNA RESTRICTION FRAGMENTS USING CAPILLARY ARRAY ELECTROPHORESIS

被引:63
作者
CLARK, SM
MATHIES, RA
机构
[1] UNIV CALIF BERKELEY,DEPT CHEM,BERKELEY,CA 94720
[2] UNIV CALIF BERKELEY,GRAD GRP BIOPHYS,BERKELEY,CA 94720
关键词
D O I
10.1006/abio.1993.1571
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new method for performing high-speed, high-throughput sizing of DNA has been developed. Samples containing DNA restriction fragments between 70 and 10,000 base pairs in length are electrophoretically separated using capillary arrays in ˜20 min and detected with high sensitivity using a fluorescence detection system. The separations of ΦX174/HaeIII fragments are performed on an array of seven 100-μm i.d., 350-μm o.d. capillaries using replaceable hydroxyethyl-cellulose solutions as the sieving medium. The fragments are fluorescently labeled using ethidium bromide in the running buffer and detected with a laser-excited, confocal-fluorescence scanner. The limit of detection is ˜1 pg of DNA per band and separations can be detected injecting DNA samples as dilute as 0.1 ng/μl. Samples were electrokinetically injected from a cassette of microcentrifuge tubes using a format that will facilitate the application of capillary electrophoresis to separations in molecular biology. The feasibility of extending this technique to lower DNA concentrations and to ˜100 capillary arrays is discussed. © 1993 Academic Press, Inc.
引用
收藏
页码:163 / 170
页数:8
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