Real-time detection of allele-specific polymerase chain reaction products by automated ultra-thin-layer agarose gel electrophoresis
Ultra-thin-layer agarose gel electrophoresis, a novel combination of agarose slab gel electrophoresis and capillary gel electrophoresis was introduced in conjunction with laser-induced fluorescence (LIF) scanning detection for the analysis of polymerase chain reaction (PCR) products. Allele-specific...
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Veröffentlicht in: | Journal of Chromatography A 1998-12, Vol.828 (1), p.481-487 |
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description | Ultra-thin-layer agarose gel electrophoresis, a novel combination of agarose slab gel electrophoresis and capillary gel electrophoresis was introduced in conjunction with laser-induced fluorescence (LIF) scanning detection for the analysis of polymerase chain reaction (PCR) products. Allele-specific fragments, amplified from genomic DNA of patients with congenital adrenal hyperplasia (most often caused by mutations of 21-hydroxylase gene, CYP-21), were used as a model system to investigate the applicability, sensitivity and resolving power of the method. The allele-specific products were generated by PCR and separated by ultra-thin-layer agarose gel electrophoresis. The double-stranded DNA fragments were easily visualized in real-time via complexation during the separation process by the intercalator dye TO-PRO-3 which was part of the separation gel–buffer system. In this way, the migrating dsDNA–dye complexes were detected in real-time by a scanning LIF detection system with sub-nanogram sensitivity. The system employs a 632-nm solid-state laser and an avalanche photodiode detector scanning to the separation platform by means of a fiber bundle system. Automated ultra-thin-layer agarose gel electrophoresis with `on the fly' TO-PRO-3 staining of dsDNA fragments and LIF detection system proved to be a very fast, high-throughput separation method for individual or multiplexed PCR products, with excellent sensitivity. |
doi_str_mv | 10.1016/S0021-9673(98)00814-0 |
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Allele-specific fragments, amplified from genomic DNA of patients with congenital adrenal hyperplasia (most often caused by mutations of 21-hydroxylase gene, CYP-21), were used as a model system to investigate the applicability, sensitivity and resolving power of the method. The allele-specific products were generated by PCR and separated by ultra-thin-layer agarose gel electrophoresis. The double-stranded DNA fragments were easily visualized in real-time via complexation during the separation process by the intercalator dye TO-PRO-3 which was part of the separation gel–buffer system. In this way, the migrating dsDNA–dye complexes were detected in real-time by a scanning LIF detection system with sub-nanogram sensitivity. The system employs a 632-nm solid-state laser and an avalanche photodiode detector scanning to the separation platform by means of a fiber bundle system. Automated ultra-thin-layer agarose gel electrophoresis with `on the fly' TO-PRO-3 staining of dsDNA fragments and LIF detection system proved to be a very fast, high-throughput separation method for individual or multiplexed PCR products, with excellent sensitivity.</description><identifier>ISSN: 0021-9673</identifier><identifier>DOI: 10.1016/S0021-9673(98)00814-0</identifier><identifier>PMID: 9916326</identifier><identifier>CODEN: JOCRAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Alleles ; Analytical, structural and metabolic biochemistry ; Automation ; Base Sequence ; Biological and medical sciences ; DNA ; DNA - isolation & purification ; DNA Primers ; Dna, deoxyribonucleoproteins ; Electrophoresis, Agar Gel - methods ; Electrophoresis, Capillary ; Fundamental and applied biological sciences. 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Allele-specific fragments, amplified from genomic DNA of patients with congenital adrenal hyperplasia (most often caused by mutations of 21-hydroxylase gene, CYP-21), were used as a model system to investigate the applicability, sensitivity and resolving power of the method. The allele-specific products were generated by PCR and separated by ultra-thin-layer agarose gel electrophoresis. The double-stranded DNA fragments were easily visualized in real-time via complexation during the separation process by the intercalator dye TO-PRO-3 which was part of the separation gel–buffer system. In this way, the migrating dsDNA–dye complexes were detected in real-time by a scanning LIF detection system with sub-nanogram sensitivity. The system employs a 632-nm solid-state laser and an avalanche photodiode detector scanning to the separation platform by means of a fiber bundle system. Automated ultra-thin-layer agarose gel electrophoresis with `on the fly' TO-PRO-3 staining of dsDNA fragments and LIF detection system proved to be a very fast, high-throughput separation method for individual or multiplexed PCR products, with excellent sensitivity.</description><subject>Alleles</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Automation</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>DNA</subject><subject>DNA - isolation & purification</subject><subject>DNA Primers</subject><subject>Dna, deoxyribonucleoproteins</subject><subject>Electrophoresis, Agar Gel - methods</subject><subject>Electrophoresis, Capillary</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Lasers</subject><subject>Nucleic acids</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometry, Fluorescence - methods</subject><issn>0021-9673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9rFTEUxWeh1Nr6EQpZiOgimmRmkslKpPgPCkJb1-FOcqcvkpmMSabw1n5x075HXbq6cO855x5-TXPB2XvOuPxww5jgVEvVvtXDO8YG3lH2rDl9Wr9oXub8izGumBInzYnWXLZCnjZ_rhECLX5G4rCgLT4uJE4EQsCANK9o_eQtWWPYz5ggI7E78AtJCAfxmqLbbMlk3BPYSpyhoCNbKAlo2fmFBthjInAHKVb3HQZSk21Jcd3FhNnn8-b5BCHjq-M8a35--Xx7-Y1e_fj6_fLTFbXtoAuVY-9QjRoGoTrHJY6KW9CAHRPgRDc5JUQvJZNKSwEDCs05up4hsrGDrj1r3hxya-XfG-ZiZp8thgALxi0bqXnXCiarsD8Iba2cE05mTX6GtDecmQfg5hG4eSBr9GAegRtWfRfHB9s4o3tyHWnX--vjHbKFMCVYrM__wqUauOyr7ONBhhXGvcdksvW4WHQ-VXDGRf-fIn8BYwehzA</recordid><startdate>19981218</startdate><enddate>19981218</enddate><creator>Guttman, András</creator><creator>Barta, Csaba</creator><creator>Szöke, Melinda</creator><creator>Sasvári-Székely, Mária</creator><creator>Kalász, Huba</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19981218</creationdate><title>Real-time detection of allele-specific polymerase chain reaction products by automated ultra-thin-layer agarose gel electrophoresis</title><author>Guttman, András ; Barta, Csaba ; Szöke, Melinda ; Sasvári-Székely, Mária ; Kalász, Huba</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-6b5de7b9a8274d16eb71ca9ae402ad24fd722566067962a8e2911ed50ee0b4a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Alleles</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Automation</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>DNA</topic><topic>DNA - isolation & purification</topic><topic>DNA Primers</topic><topic>Dna, deoxyribonucleoproteins</topic><topic>Electrophoresis, Agar Gel - methods</topic><topic>Electrophoresis, Capillary</topic><topic>Fundamental and applied biological sciences. 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Allele-specific fragments, amplified from genomic DNA of patients with congenital adrenal hyperplasia (most often caused by mutations of 21-hydroxylase gene, CYP-21), were used as a model system to investigate the applicability, sensitivity and resolving power of the method. The allele-specific products were generated by PCR and separated by ultra-thin-layer agarose gel electrophoresis. The double-stranded DNA fragments were easily visualized in real-time via complexation during the separation process by the intercalator dye TO-PRO-3 which was part of the separation gel–buffer system. In this way, the migrating dsDNA–dye complexes were detected in real-time by a scanning LIF detection system with sub-nanogram sensitivity. The system employs a 632-nm solid-state laser and an avalanche photodiode detector scanning to the separation platform by means of a fiber bundle system. Automated ultra-thin-layer agarose gel electrophoresis with `on the fly' TO-PRO-3 staining of dsDNA fragments and LIF detection system proved to be a very fast, high-throughput separation method for individual or multiplexed PCR products, with excellent sensitivity.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9916326</pmid><doi>10.1016/S0021-9673(98)00814-0</doi><tpages>7</tpages></addata></record> |
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subjects | Alleles Analytical, structural and metabolic biochemistry Automation Base Sequence Biological and medical sciences DNA DNA - isolation & purification DNA Primers Dna, deoxyribonucleoproteins Electrophoresis, Agar Gel - methods Electrophoresis, Capillary Fundamental and applied biological sciences. Psychology Humans Lasers Nucleic acids Polymerase Chain Reaction - methods Sensitivity and Specificity Spectrometry, Fluorescence - methods |
title | Real-time detection of allele-specific polymerase chain reaction products by automated ultra-thin-layer agarose gel electrophoresis |
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