High-speed screening of polymerase chain reaction products by capillary electrophoresis

被引:22
作者
Chan, KC [1 ]
Muschik, CM [1 ]
Issaq, HJ [1 ]
Garvey, KJ [1 ]
Generlette, PL [1 ]
机构
[1] NCI, RECOMBINANT DNA LAB, SAIC FREDERICK, FREDERICK CANC RES & DEV CTR, FREDERICK, MD 21702 USA
关键词
D O I
10.1006/abio.1996.0491
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In an effort to develop capillary electrophoresis (CE) for high-throughput polymerase chain reaction (PCR) molecular diagnostics, a method was developed to rapidly screen small PCR products of similar molecular weights. The assay of interest required the separation of two PCR products (375 and 400 bp) in an assay of TGF-beta(1) knockout mice to determine the genotype of neonates. Using a commercially available CE instrument, the two PCR products were separated in 12 min with a replaceable gel buffer, a 20-cm effective length DB-17 capillary, and 185 V/cm field strength. With the coinjection of a 20-bp ladder, the sizes of the PCR products were determined hom the electropherogram without using a calibration plot and curve-fitting program. Faster separation was obtained using the combination of a short effective length capillary and high field strength. The two PCR products were separated in 82 s with a 7-cm effective length capillary and 556 V/cm. A 60% buffer further reduced the separation time in about a minute. This high-speed separation, with minimum postrun data processing, is highly desirable for the high-throughput screening of PCR products using a single-capillary CE system. (C) 1996 Academic Press, Inc.
引用
收藏
页码:133 / 139
页数:7
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