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High-throughput isolation of ultra-pure plasmid DNA by a robotic system
BACKGROUND: With the availability of complete genomes, a systematic inventory of cellular processes becomes achievable. This requires assessing the function of all individual genes. Transfection of plasmid DNA into cell culture cells is an essential technique for this aim as it allows functional ove...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1395312/ https://www.ncbi.nlm.nih.gov/pubmed/16483377 http://dx.doi.org/10.1186/1472-6750-6-9 |
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author | Kachel, Volker Sindelar, Georg Grimm, Stefan |
author_facet | Kachel, Volker Sindelar, Georg Grimm, Stefan |
author_sort | Kachel, Volker |
collection | PubMed |
description | BACKGROUND: With the availability of complete genomes, a systematic inventory of cellular processes becomes achievable. This requires assessing the function of all individual genes. Transfection of plasmid DNA into cell culture cells is an essential technique for this aim as it allows functional overexpression or downregulation of genes. While many robotic systems isolate plasmids for sequencing purposes, for more demanding applications such as transfections there is a shortage of robots for the high-throughput isolation of plasmid DNA. RESULTS: Here we describe a custom-made, automated device, which uses a special protocol to isolate plasmid DNAs with a purity sufficient for efficient transfections into mammalian cells. Approximately 1,600 ultra pure plasmids can be isolated in a 96-well plate format within 12 hours. As a unique feature the robot comprises the integration of a centrifuge instead of expensive columns, the use of a custom-made pipetting head with a movable gripper, especially designed shaking platforms and an acetone wash facility. CONCLUSION: Using this robot we demonstrate how centrifugation steps with multiple precipitations, most notably through a precipitation step of SDS in isopropanol, lead to high purity plasmid DNA and make possible high-throughput transfections into mammalian cells for functional gene annotations. |
format | Text |
id | pubmed-1395312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-13953122006-03-09 High-throughput isolation of ultra-pure plasmid DNA by a robotic system Kachel, Volker Sindelar, Georg Grimm, Stefan BMC Biotechnol Methodology Article BACKGROUND: With the availability of complete genomes, a systematic inventory of cellular processes becomes achievable. This requires assessing the function of all individual genes. Transfection of plasmid DNA into cell culture cells is an essential technique for this aim as it allows functional overexpression or downregulation of genes. While many robotic systems isolate plasmids for sequencing purposes, for more demanding applications such as transfections there is a shortage of robots for the high-throughput isolation of plasmid DNA. RESULTS: Here we describe a custom-made, automated device, which uses a special protocol to isolate plasmid DNAs with a purity sufficient for efficient transfections into mammalian cells. Approximately 1,600 ultra pure plasmids can be isolated in a 96-well plate format within 12 hours. As a unique feature the robot comprises the integration of a centrifuge instead of expensive columns, the use of a custom-made pipetting head with a movable gripper, especially designed shaking platforms and an acetone wash facility. CONCLUSION: Using this robot we demonstrate how centrifugation steps with multiple precipitations, most notably through a precipitation step of SDS in isopropanol, lead to high purity plasmid DNA and make possible high-throughput transfections into mammalian cells for functional gene annotations. BioMed Central 2006-02-16 /pmc/articles/PMC1395312/ /pubmed/16483377 http://dx.doi.org/10.1186/1472-6750-6-9 Text en Copyright © 2006 Kachel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Kachel, Volker Sindelar, Georg Grimm, Stefan High-throughput isolation of ultra-pure plasmid DNA by a robotic system |
title | High-throughput isolation of ultra-pure plasmid DNA by a robotic system |
title_full | High-throughput isolation of ultra-pure plasmid DNA by a robotic system |
title_fullStr | High-throughput isolation of ultra-pure plasmid DNA by a robotic system |
title_full_unstemmed | High-throughput isolation of ultra-pure plasmid DNA by a robotic system |
title_short | High-throughput isolation of ultra-pure plasmid DNA by a robotic system |
title_sort | high-throughput isolation of ultra-pure plasmid dna by a robotic system |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1395312/ https://www.ncbi.nlm.nih.gov/pubmed/16483377 http://dx.doi.org/10.1186/1472-6750-6-9 |
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