Literature DB >> 11870770

Rapid microwell polymerase chain reaction with subsequent ultrathin-layer gel electrophoresis of DNA.

Sarah Shandrick1, Zsolt Ronai, András Guttman.   

Abstract

Large-scale genotyping, mapping and expression profiling require affordable, fully automated high-throughput devices enabling rapid, high-performance analysis using minute quantities of reagents. In this paper, we describe a new combination of microwell polymerase chain reaction (PCR) based DNA amplification technique with automated ultrathin-layer gel electrophoresis analysis of the resulting products. This technique decreases the reagent consumption (total reaction volume 0.75-1 microL), the time requirement of the PCR (15-20 min) and subsequent ultrathin-layer gel electrophoresis based fragment analysis (5 min) by automating the current manual procedure and reducing the human intervention using sample loading robots and computerized real time data analysis. Small aliquots (0.2 microL) of the submicroliter size PCR reaction were transferred onto loading membranes and analyzed by ultrathin-layer gel electrophoresis which is a novel, high-performance and automated microseparation technique. This system employs integrated scanning laser-induced fluorescence-avalanche photodiode detection and combines the advantages of conventional slab and capillary gel electrophoresis. Visualization of the DNA fragments was accomplished by "in migratio" complexation with ethidium bromide during the electrophoresis process also enabling real time imaging and data analysis.

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Year:  2002        PMID: 11870770     DOI: 10.1002/1522-2683(200202)23:4<591::AID-ELPS591>3.0.CO;2-W

Source DB:  PubMed          Journal:  Electrophoresis        ISSN: 0173-0835            Impact factor:   3.535


  2 in total

1.  Investigating DNA migration in pulsed fields using a miniaturized FIGE system.

Authors:  Xiaojia Chen; Victor M Ugaz
Journal:  Electrophoresis       Date:  2008-12       Impact factor: 3.535

2.  Direct chromatin PCR (DC-PCR): hypotonic conditions allow differentiation of chromatin states during thermal cycling.

Authors:  Sergei Vatolin; Shahper N Khan; Frederic J Reu
Journal:  PLoS One       Date:  2012-09-12       Impact factor: 3.240

  2 in total

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