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Integrated allele-specific polymerase chain reaction-capillary electrophoresis microdevice for single nucleotide polymorphism genotyping

  • Jong Young Choi
  • , Yong Tae Kim
  • , Jinwoo Ahn
  • , Kwan Suk Kim
  • , Dae Gab Gweon
  • , Tae Seok Seo

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

An integrated allele-specific (AS) polymerase chain reaction (PCR) and capillary electrophoresis (CE) microdevice has been developed for multiplex single nucleotide polymorphism (SNP) genotyping on a portable instrumentation, which was applied for on-site identification of HANWOO (Korean indigenous beef cattle). Twelve sets of primers were designed for targeting beef cattle's eleven SNP loci for HANWOO verification and one primer set for a positive PCR control, and the success rate for identification of HANWOO was demonstrated statistically. The AS PCR and CE separation for multiplex SNP typing was carried out on a glass-based microchip consisting of four layers: a microchannel plate for microfluidic control, a Pt-electrode plate for a resistance temperature detector (RTD), a poly(dimethylsiloxane) (PDMS) membrane and a manifold glass for microvalve function. The operation of the sample loading, AS PCR, microvalve, and CE on a chip was automated with a portable genetic analyzer, and the laser-induced fluorescence detection was performed on a miniaturized fluorescence detector. The blind samples were correctly identified as a HANWOO by showing one or two amplicon peaks in the electropherogram, while the imported beef cattle revealed more than five peaks. Our genetic analysis platform provides rapid, accurate, and on-site multiplex SNP typing.

Original languageEnglish
Pages (from-to)327-334
Number of pages8
JournalBiosensors and Bioelectronics
Volume35
Issue number1
DOIs
Publication statusPublished - 15 May 2012

Bibliographical note

Funding Information:
This work was supported by Technology Development Program for Agriculture and Forestry , Ministry for Agriculture, Forestry and Fisheries , and also partially by the Ministry of Knowledge Economy (No. 10035638 ), Republic of Korea. In addition, the authors would like to thank Nanoscope Systems Inc. for supporting experimental instrumentation, and Solgent Co., Ltd. for preparing this manuscript.

Keywords

  • Allele-specific polymerase chain reaction
  • Capillary electrophoresis
  • Integrated microdevice
  • On-site detection
  • Single nucleotide polymorphism

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