Automated high multiplex qPCR platform for simultaneous detection and quantification of multiple nucleic acid targets
Author(s) -
Louis Hlousek,
Sergey Voronov,
Vesselin Diankov,
Amy B. Leblang,
Patrick J. Wells,
Donna M. Ford,
Jörk Nölling,
Kyle W. Hart,
Patricio Espinoza,
Michael R. Bristol,
Gregory J. Tsongalis,
Belinda YenLieberman,
Vladimir I. Slepnev,
Lilly I. Kong,
Ming-Chou Lee
Publication year - 2012
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/0000113852
Subject(s) - amplicon , multiplex , nucleic acid , biology , multiplex polymerase chain reaction , real time polymerase chain reaction , computational biology , polymerase chain reaction , microbiology and biotechnology , gene , genetics
Quantitative PCR (qPCR) using real-time detection of amplification is limited to a small number of targets within a single reaction. The ICEPlex system, using our scalable target analysis routine (STAR) technology, was developed to provide an automated, high multiplexing PCR solution. ICEPlex combines PCR thermal cycling with dynamic, sequential amplicon separation by capillary electrophoresis and two-color quantitative detection in a single integrated system. In contrast to probe-based qPCR, ICEPlex directly measures amplicon accumulation through incorporation of labeled primers. Three orders of magnitude of optical detection range and at least 7 logs of detectable target concentration range are demonstrated. The system can separate more than 50 amplicons per color channel, ranging from 100 to 500 bases, providing broad multiplexing capabilities for a wide spectrum of nucleic acid amplification applications. ICEPlex can be used for analysis of viral DNA or RNA targets, detection of genetic variants, and for reverse-transcriptase PCR gene expression panels.
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