Literature DB >> 22578124

Automated high multiplex qPCR platform for simultaneous detection and quantification of multiple nucleic acid targets.

Louis Hlousek1, Sergey Voronov, Vesselin Diankov, Amy B Leblang, Patrick J Wells, Donna M Ford, Jork Nolling, Kyle W Hart, Patricio A Espinoza, Michael R Bristol, Gregory J Tsongalis, Belinda Yen-Lieberman, Vladimir I Slepnev, Lilly I Kong, Ming-Chou Lee.   

Abstract

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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Year:  2012        PMID: 22578124     DOI: 10.2144/0000113852

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  5 in total

1.  Employment of Near Full-Length Ribosome Gene TA-Cloning and Primer-Blast to Detect Multiple Species in a Natural Complex Microbial Community Using Species-Specific Primers Designed with Their Genome Sequences.

Authors:  Huimin Zhang; Hongkui He; Xiujuan Yu; Zhaohui Xu; Zhizhou Zhang
Journal:  Mol Biotechnol       Date:  2016-11       Impact factor: 2.695

2.  Comparison of a transplant multiplex viral panel on the ICEPlex system with real-time PCR for detection of cytomegalovirus, Epstein-Barr virus, and BK virus in clinical specimens.

Authors:  Reeti Khare; Mark J Espy; Jayawant N Mandrekar; Matthew J Binnicker
Journal:  J Clin Microbiol       Date:  2014-02-19       Impact factor: 5.948

3.  Molecular subtype classification of formalin-fixed, paraffin-embedded diffuse large B-cell lymphoma samples on the ICEPlex® system.

Authors:  Angela M B Collie; Jörk Nölling; Kiran M Divakar; Jeffrey J Lin; Paula Carver; Lisa M Durkin; Brian T Hill; Mitchell R Smith; Tomas Radivoyevitch; Lilly I Kong; Thomas Daly; Gurunathan Murugesan; Jeanna Guenther-Johnson; Sandeep S Dave; Elena A Manilich; Eric D Hsi
Journal:  Br J Haematol       Date:  2014-06-25       Impact factor: 6.998

4.  Molecular assessment of trematode co-infection and intraspecific competition in molluscan intermediate hosts.

Authors:  Elizabeth A Thiele; Dennis J Minchella
Journal:  Mol Biochem Parasitol       Date:  2012-12-20       Impact factor: 1.759

5.  Highly multiplex PCR assays by coupling the 5'-flap endonuclease activity of Taq DNA polymerase and molecular beacon reporters.

Authors:  Qiuying Huang; Dongmei Chen; Chen Du; Qiaoqiao Liu; Su Lin; Lanlan Liang; Ye Xu; Yiqun Liao; Qingge Li
Journal:  Proc Natl Acad Sci U S A       Date:  2022-03-01       Impact factor: 12.779

  5 in total

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