Treatment of long-term stored DNA- Comparison between different methods to obtain high-quality materia

dc.contributor.authorAlmeida, Maira Pedroso de
dc.contributor.authorNascimento, Carlos Souza do
dc.contributor.authorPerissé, Iuri Viotti
dc.contributor.authorDuarte, Marcio de Souza
dc.contributor.authorVeroneze, Renata
dc.contributor.authorGuimarães, Simone E. Facioni
dc.date.accessioned2018-01-02T10:18:30Z
dc.date.available2018-01-02T10:18:30Z
dc.date.issued2013-07-03
dc.description.abstractLong-term stored DNA can be sometimes the only source of genetic material of an organism that does not exist anymore, but a research interest still persists. However, there is a lack of information about useful methods to improve quality from such type of material. In this study, we compared four different protocols using DNA samples collected in 1998. Fresh DNA was also tested aiming to check the differences between these two material types. Sixteen samples of each DNA type treated with phenol-chloroform with PEG 5.0%, silica-gel membrane spin column, PEG 7.5%, and glass-fiber matrix spin column were submitted to spectrophotometer measurements, electrophoresis, PCR, and RFLP-PCR to assess the best method concerning yield, quality, and purity. Based on the results, purification with PEG 7.5% was considered the best method to treat aged DNA samples. In addition to the efficiency, this protocol has low cost. Analyzing the data, we also conclude that long-term stored DNA may be considered a reliable and potential resource for future molecular studies.Long-term stored DNA can be sometimes the only source of genetic material of an organism that does not exist anymore, but a research interest still persists. However, there is a lack of information about useful methods to improve quality from such type of material. In this study, we compared four different protocols using DNA samples collected in 1998. Fresh DNA was also tested aiming to check the differences between these two material types. Sixteen samples of each DNA type treated with phenol-chloroform with PEG 5.0%, silica-gel membrane spin column, PEG 7.5%, and glass-fiber matrix spin column were submitted to spectrophotometer measurements, electrophoresis, PCR, and RFLP-PCR to assess the best method concerning yield, quality, and purity. Based on the results, purification with PEG 7.5% was considered the best method to treat aged DNA samples. In addition to the efficiency, this protocol has low cost. Analyzing the data, we also conclude that long-term stored DNA may be considered a reliable and potential resource for future molecular studies.en
dc.formatpdfpt-BR
dc.identifier.issn1539-3704
dc.identifier.urihttp://dx.doi.org/10.1002/elps.201300245
dc.identifier.urihttp://www.locus.ufv.br/handle/123456789/16039
dc.language.isoengpt-BR
dc.publisherPubMedpt-BR
dc.relation.ispartofseriesv. 34, Issue 20-21. p. 3039–3045, November 2013pt-BR
dc.rightsOpen Accesspt-BR
dc.subjectDNA purificationpt-BR
dc.subjectLong-term storagept-BR
dc.subjectPolymerase chain reactionpt-BR
dc.titleTreatment of long-term stored DNA- Comparison between different methods to obtain high-quality materiaen
dc.typeArtigopt-BR

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