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Filter paper-based spin column method for cost-efficient DNA or RNA purification
We describe herein a method of recharging used commercial spin columns or assembling homemade spin columns using filter paper as binding material for cost-effective, low throughput nucleic acid purification. The efficiency of filter paper-based spin columns was evaluated for purification of nucleic...
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Published in: | PloS one 2018-12, Vol.13 (12), p.e0203011-e0203011 |
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description | We describe herein a method of recharging used commercial spin columns or assembling homemade spin columns using filter paper as binding material for cost-effective, low throughput nucleic acid purification. The efficiency of filter paper-based spin columns was evaluated for purification of nucleic acids from various sources. Following protocols of commercial kits, we found filter paper to be a useful binding material for purification of nucleic acids, including plant genomic DNA, plant total RNA, PCR products, and DNA from agarose gels. However, filter paper has a weak binding affinity to plasmid DNA in tested miniprep protocols. Protocols for the use of filter paper recharged spin columns or homemade spin columns for low throughput purification of plant genomic DNA and total RNA with unused commercial kit buffers or less expensive homemade buffers are presented. |
doi_str_mv | 10.1371/journal.pone.0203011 |
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The efficiency of filter paper-based spin columns was evaluated for purification of nucleic acids from various sources. Following protocols of commercial kits, we found filter paper to be a useful binding material for purification of nucleic acids, including plant genomic DNA, plant total RNA, PCR products, and DNA from agarose gels. However, filter paper has a weak binding affinity to plasmid DNA in tested miniprep protocols. Protocols for the use of filter paper recharged spin columns or homemade spin columns for low throughput purification of plant genomic DNA and total RNA with unused commercial kit buffers or less expensive homemade buffers are presented.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0203011</identifier><identifier>PMID: 30532193</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Backup software ; Binding ; Biology and Life Sciences ; Buffers ; Cellulose ; Centrifugation - methods ; Crops ; Deoxyribonucleic acid ; DNA ; DNA, Plant - chemistry ; DNA, Plant - isolation & purification ; Economic aspects ; Engineering and Technology ; Filter paper ; Gels ; Horticulture ; Laboratories ; Methods ; Molecular biology ; Nicotiana - chemistry ; Nucleic acids ; Physical Sciences ; Plasmids ; Purification ; Recharging ; Research and analysis methods ; Ribonucleic acid ; RNA ; RNA, Plant - chemistry ; RNA, Plant - isolation & purification ; Soil sciences ; Solanum lycopersicum - chemistry ; Tobacco</subject><ispartof>PloS one, 2018-12, Vol.13 (12), p.e0203011-e0203011</ispartof><rights>COPYRIGHT 2018 Public Library of Science</rights><rights>This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication: https://creativecommons.org/publicdomain/zero/1.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c585t-3250a28bcff21585a45cb9e035a2479fbbc55659fc779f0ad9aa9b4415441dc33</citedby><cites>FETCH-LOGICAL-c585t-3250a28bcff21585a45cb9e035a2479fbbc55659fc779f0ad9aa9b4415441dc33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2151747137/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2151747137?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,75096</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30532193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Rui</creatorcontrib><creatorcontrib>Lewis, Ramsey S</creatorcontrib><creatorcontrib>Panthee, Dilip R</creatorcontrib><title>Filter paper-based spin column method for cost-efficient DNA or RNA purification</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>We describe herein a method of recharging used commercial spin columns or assembling homemade spin columns using filter paper as binding material for cost-effective, low throughput nucleic acid purification. The efficiency of filter paper-based spin columns was evaluated for purification of nucleic acids from various sources. Following protocols of commercial kits, we found filter paper to be a useful binding material for purification of nucleic acids, including plant genomic DNA, plant total RNA, PCR products, and DNA from agarose gels. However, filter paper has a weak binding affinity to plasmid DNA in tested miniprep protocols. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Rui</au><au>Lewis, Ramsey S</au><au>Panthee, Dilip R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Filter paper-based spin column method for cost-efficient DNA or RNA purification</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-12-07</date><risdate>2018</risdate><volume>13</volume><issue>12</issue><spage>e0203011</spage><epage>e0203011</epage><pages>e0203011-e0203011</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>We describe herein a method of recharging used commercial spin columns or assembling homemade spin columns using filter paper as binding material for cost-effective, low throughput nucleic acid purification. The efficiency of filter paper-based spin columns was evaluated for purification of nucleic acids from various sources. Following protocols of commercial kits, we found filter paper to be a useful binding material for purification of nucleic acids, including plant genomic DNA, plant total RNA, PCR products, and DNA from agarose gels. However, filter paper has a weak binding affinity to plasmid DNA in tested miniprep protocols. Protocols for the use of filter paper recharged spin columns or homemade spin columns for low throughput purification of plant genomic DNA and total RNA with unused commercial kit buffers or less expensive homemade buffers are presented.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>30532193</pmid><doi>10.1371/journal.pone.0203011</doi><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Backup software Binding Biology and Life Sciences Buffers Cellulose Centrifugation - methods Crops Deoxyribonucleic acid DNA DNA, Plant - chemistry DNA, Plant - isolation & purification Economic aspects Engineering and Technology Filter paper Gels Horticulture Laboratories Methods Molecular biology Nicotiana - chemistry Nucleic acids Physical Sciences Plasmids Purification Recharging Research and analysis methods Ribonucleic acid RNA RNA, Plant - chemistry RNA, Plant - isolation & purification Soil sciences Solanum lycopersicum - chemistry Tobacco |
title | Filter paper-based spin column method for cost-efficient DNA or RNA purification |
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