Comparison of slab gel electrophoresis and capillary electrophoresis for the detection of the fluorescently labeled polymerase chain reaction products of short tandem repeat fragments

被引:35
作者
Deforce, DLD [1 ]
Millecamps, REM [1 ]
Van Hoofstat, D [1 ]
Van den Eeckhout, EG [1 ]
机构
[1] State Univ Ghent, Pharmaceut Biotechnol Lab, B-9000 Ghent, Belgium
关键词
polymerase chain reaction; short tandem repeat fragments; nucleotides;
D O I
10.1016/S0021-9673(97)00394-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The sizing capability of slab gel electrophoresis for short tandem repeat (STR) fragments was compared to the sizing capability of capillary electrophoresis (CE). Both systems used automated laser fluorescence detection to detect four fluorescent dyes, enabling the use of an internal lane standard within each sample. The STR fragments were amplified using a multiplex polymerase chain reaction (PCR) in which the STR fragments Hum CD-4, Hum TH01, Hum D21S11 and Hum SE33 were amplified simultaneously. The reproducibility of the size calling was determined for both systems. The average standard deviation obtained for the slab gel system was 0.2, which was comparable to the standard deviation of 0.12 obtained for the CE system. The CE system produced results comparable to those obtained on the slab gel system, with a level of precision of +/-1.0 bp (between instruments). (C) 1998 Published by Elsevier Science B.V.
引用
收藏
页码:149 / 155
页数:7
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