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dc.contributor.authorTzakos, A. G.en
dc.contributor.authorEaston, L. E.en
dc.contributor.authorLukavsky, P. J.en
dc.date.accessioned2015-11-24T16:54:12Z-
dc.date.available2015-11-24T16:54:12Z-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10128-
dc.rightsDefault Licence-
dc.subjectCarbon Isotopesen
dc.subjectImines/chemistryen
dc.subjectIsotope Labeling/*methodsen
dc.subjectMagnetic Resonance Spectroscopy/methodsen
dc.subjectNitrogen Isotopesen
dc.subjectNucleic Acid Conformationen
dc.subjectPharmaceutical Preparations/*chemical synthesis/*economicsen
dc.subjectRNA/*chemistryen
dc.subjectTranscription, Geneticen
dc.titleComplementary segmental labeling of large RNAs: economic preparation and simplified NMR spectra for measurement of more RDCsen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1021/ja064807o-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/17031932-
heal.identifier.secondaryhttp://pubs.acs.org/doi/pdfplus/10.1021/ja064807o-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2006-
heal.abstractNMR structure determination of large RNAs is often restricted by limited RDC information caused by chemical shift degeneracy. We established a general, time- and cost-effective methodology for the preparation of 13C/15N complementary labeled RNAs from a single plasmid. Applying this method to the 25 kDa BC1-DTE RNA, we were able to resolve severe chemical shift degeneracy, thereby almost doubling the number of RDC restraints in comparison to the conventional 13C,15N uniform-labeled RNA.en
heal.publisherAmerican Chemical Societyen
heal.journalNameJ Am Chem Socen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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