نمایش مختصر رکورد

dc.contributor.authorMajidi, Mohammaden_US
dc.contributor.authorBahmani, Yonesen_US
dc.date.accessioned1399-07-08T19:18:53Zfa_IR
dc.date.accessioned2020-09-29T19:18:53Z
dc.date.available1399-07-08T19:18:53Zfa_IR
dc.date.available2020-09-29T19:18:53Z
dc.date.issued2017-12-01en_US
dc.date.issued1396-09-10fa_IR
dc.date.submitted2018-02-23en_US
dc.date.submitted1396-12-04fa_IR
dc.identifier.citationMajidi, Mohammad, Bahmani, Yones. (2017). Isolation of high-quality RNA from a wide range of woody plants. Journal of Plant Molecular Breeding, 5(2), 50-59. doi: 10.22058/jpmb.2018.82001.1157en_US
dc.identifier.issn2322-3332
dc.identifier.issn2322-5092
dc.identifier.urihttps://dx.doi.org/10.22058/jpmb.2018.82001.1157
dc.identifier.urihttp://www.jpmb-gabit.ir/article_31194.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/63912
dc.description.abstractIsolation of high-quality RNA is one of the most crucial methods in molecular biology. RNA extraction from woody plants has been problematic due to the presence of rigid and woody tissues, large amounts of polysaccharides, polyphenols and other secondary metabolites. Here we present a suitable protocol for RNA isolation from a wide range of woody plants that includes eight gymnosperms and four angiosperms. The method is based on the CTAB protocol which was modified by adding sodium citrate and two helper buffers. Agarose gel electrophoresis showed a good RNA integrity and total RNA profile that includes all expected RNA bands. Also, DNA and protein contaminations were not observed. Spectrophotometric quantification of RNA samples by NanoDrop showed that the average RNA yields ranged from 35.68 to 216.98 µg per gram fresh weight, that is enough to proceed into cDNA synthesis and other RNA-related works. Both the A260/A280 and A260/A230 ratios were in the desired ranges, indicating that RNA was of high purity and without protein, polyphenol, and polysaccharide contamination. The efficiency of isolated RNA for downstream applications was verified by real-time PCR and successful amplification of a long cDNA. Finally, some advantages and possible applications of the method are also mentioned.en_US
dc.format.extent1662
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherGenetics and Agricultural Biotechnology Institute of Tabarestan (GABIT)en_US
dc.relation.ispartofJournal of Plant Molecular Breedingen_US
dc.relation.isversionofhttps://dx.doi.org/10.22058/jpmb.2018.82001.1157
dc.subjectRNA isolationen_US
dc.subjectWoody plantsen_US
dc.subjectContaminationsen_US
dc.subjectCTABen_US
dc.subjectSodium citrateen_US
dc.subjectHelper buffersen_US
dc.subjectGenetic engineering & plant breedingen_US
dc.titleIsolation of high-quality RNA from a wide range of woody plantsen_US
dc.typeTexten_US
dc.typeResearch Paperen_US
dc.contributor.departmentDepartment of Biotechnology, Faculty of Agriculture, Azarbaijan Shahid Madani University, Tabriz, Iranen_US
dc.contributor.departmentDepartment of Biotechnology, Faculty of Agriculture, Azarbaijan Shahid Madani University, Tabriz, Iranen_US
dc.citation.volume5
dc.citation.issue2
dc.citation.spage50
dc.citation.epage59


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