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GC Preps: Fast and Easy Extraction of Stable Yeast Genomic DNA
Existing yeast genomic DNA extraction methods are not ideally suited to extensive screening of colonies by PCR, due to being too lengthy, too laborious or yielding poor quality DNA and inconsistent results. We developed the GC prep method as a solution to this problem. Yeast cells from colonies or l...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886510/ https://www.ncbi.nlm.nih.gov/pubmed/27240644 http://dx.doi.org/10.1038/srep26863 |
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author | Blount, Benjamin A. Driessen, Maureen R. M. Ellis, Tom |
author_facet | Blount, Benjamin A. Driessen, Maureen R. M. Ellis, Tom |
author_sort | Blount, Benjamin A. |
collection | PubMed |
description | Existing yeast genomic DNA extraction methods are not ideally suited to extensive screening of colonies by PCR, due to being too lengthy, too laborious or yielding poor quality DNA and inconsistent results. We developed the GC prep method as a solution to this problem. Yeast cells from colonies or liquid cultures are lysed by vortex mixing with glass beads and then boiled in the presence of a metal chelating resin. In around 12 minutes, multiple samples can be processed to extract high yields of genomic DNA. These preparations perform as effectively in PCR screening as DNA purified by organic solvent methods, are stable for up to 1 year at room temperature and can be used as the template for PCR amplification of fragments of at least 8 kb. |
format | Online Article Text |
id | pubmed-4886510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48865102016-06-08 GC Preps: Fast and Easy Extraction of Stable Yeast Genomic DNA Blount, Benjamin A. Driessen, Maureen R. M. Ellis, Tom Sci Rep Article Existing yeast genomic DNA extraction methods are not ideally suited to extensive screening of colonies by PCR, due to being too lengthy, too laborious or yielding poor quality DNA and inconsistent results. We developed the GC prep method as a solution to this problem. Yeast cells from colonies or liquid cultures are lysed by vortex mixing with glass beads and then boiled in the presence of a metal chelating resin. In around 12 minutes, multiple samples can be processed to extract high yields of genomic DNA. These preparations perform as effectively in PCR screening as DNA purified by organic solvent methods, are stable for up to 1 year at room temperature and can be used as the template for PCR amplification of fragments of at least 8 kb. Nature Publishing Group 2016-05-31 /pmc/articles/PMC4886510/ /pubmed/27240644 http://dx.doi.org/10.1038/srep26863 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Blount, Benjamin A. Driessen, Maureen R. M. Ellis, Tom GC Preps: Fast and Easy Extraction of Stable Yeast Genomic DNA |
title | GC Preps: Fast and Easy Extraction of Stable Yeast Genomic DNA |
title_full | GC Preps: Fast and Easy Extraction of Stable Yeast Genomic DNA |
title_fullStr | GC Preps: Fast and Easy Extraction of Stable Yeast Genomic DNA |
title_full_unstemmed | GC Preps: Fast and Easy Extraction of Stable Yeast Genomic DNA |
title_short | GC Preps: Fast and Easy Extraction of Stable Yeast Genomic DNA |
title_sort | gc preps: fast and easy extraction of stable yeast genomic dna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886510/ https://www.ncbi.nlm.nih.gov/pubmed/27240644 http://dx.doi.org/10.1038/srep26863 |
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