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Genotyping on a Complementary Metal Oxide Semiconductor Silicon Polymerase Chain Reaction Chip with Integrated DNA Microarray
A novel method for the fast identification of genetic material utilizing a micro-DNA amplification and analysis device (μ-DAAD) consisting of multiple PCR microreactors with integrated DNA microarrays was developed. The device was fabricated in Si-technology and used for the genotyping of Chinese me...
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Published in: | Analytical chemistry (Washington) 2002-07, Vol.74 (13), p.3168-3173 |
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container_end_page | 3173 |
container_issue | 13 |
container_start_page | 3168 |
container_title | Analytical chemistry (Washington) |
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creator | Trau, Dieter Lee, Thomas M. H Lao, Alex I. K Lenigk, Ralf Hsing, I-Ming Ip, Nancy Y Carles, Maria C Sucher, Nikolaus J |
description | A novel method for the fast identification of genetic material utilizing a micro-DNA amplification and analysis device (μ-DAAD) consisting of multiple PCR microreactors with integrated DNA microarrays was developed. The device was fabricated in Si-technology and used for the genotyping of Chinese medicinal plants on the basis of differences in the noncoding region of the 5S-rRNA gene. Successful amplification of the genetic material and the consecutive analysis of the fluorescent-labeled amplicons in the μ-DAAD by the integrated oligonucleotide probes were demonstrated. Parallel analysis was performed by loading the four PCR reactors of the μ-DAAD with different samples of 3-μL volume. Temperature sensors and heating elements of the μ-DAAD enable precise temperature control and fast cycling, allowing the rapid completion of a combined amplification and analysis (hybridization) experiment. |
doi_str_mv | 10.1021/ac020053u |
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Temperature sensors and heating elements of the μ-DAAD enable precise temperature control and fast cycling, allowing the rapid completion of a combined amplification and analysis (hybridization) experiment.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/ac020053u</identifier><identifier>PMID: 12141679</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Biological and medical sciences ; CMOS integrated circuits ; Deoxyribonucleic acid ; DNA ; Fundamental and applied biological sciences. Psychology ; Genetic engineering ; Genetics ; Genotype ; Microcomputers ; Microscopy, Confocal ; Molecular and cellular biology ; Molecular genetics ; Oligonucleotide Array Sequence Analysis - instrumentation ; Oligonucleotide Probes ; Reverse Transcriptase Polymerase Chain Reaction - instrumentation ; Spectrometry, Fluorescence ; Temperature control ; Transcription. Transcription factor. Splicing. 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H</creatorcontrib><creatorcontrib>Lao, Alex I. K</creatorcontrib><creatorcontrib>Lenigk, Ralf</creatorcontrib><creatorcontrib>Hsing, I-Ming</creatorcontrib><creatorcontrib>Ip, Nancy Y</creatorcontrib><creatorcontrib>Carles, Maria C</creatorcontrib><creatorcontrib>Sucher, Nikolaus J</creatorcontrib><title>Genotyping on a Complementary Metal Oxide Semiconductor Silicon Polymerase Chain Reaction Chip with Integrated DNA Microarray</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>A novel method for the fast identification of genetic material utilizing a micro-DNA amplification and analysis device (μ-DAAD) consisting of multiple PCR microreactors with integrated DNA microarrays was developed. The device was fabricated in Si-technology and used for the genotyping of Chinese medicinal plants on the basis of differences in the noncoding region of the 5S-rRNA gene. Successful amplification of the genetic material and the consecutive analysis of the fluorescent-labeled amplicons in the μ-DAAD by the integrated oligonucleotide probes were demonstrated. Parallel analysis was performed by loading the four PCR reactors of the μ-DAAD with different samples of 3-μL volume. Temperature sensors and heating elements of the μ-DAAD enable precise temperature control and fast cycling, allowing the rapid completion of a combined amplification and analysis (hybridization) experiment.</description><subject>Biological and medical sciences</subject><subject>CMOS integrated circuits</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic engineering</subject><subject>Genetics</subject><subject>Genotype</subject><subject>Microcomputers</subject><subject>Microscopy, Confocal</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Oligonucleotide Array Sequence Analysis - instrumentation</subject><subject>Oligonucleotide Probes</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - instrumentation</subject><subject>Spectrometry, Fluorescence</subject><subject>Temperature control</subject><subject>Transcription. Transcription factor. Splicing. 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subjects | Biological and medical sciences CMOS integrated circuits Deoxyribonucleic acid DNA Fundamental and applied biological sciences. Psychology Genetic engineering Genetics Genotype Microcomputers Microscopy, Confocal Molecular and cellular biology Molecular genetics Oligonucleotide Array Sequence Analysis - instrumentation Oligonucleotide Probes Reverse Transcriptase Polymerase Chain Reaction - instrumentation Spectrometry, Fluorescence Temperature control Transcription. Transcription factor. Splicing. Rna processing |
title | Genotyping on a Complementary Metal Oxide Semiconductor Silicon Polymerase Chain Reaction Chip with Integrated DNA Microarray |
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