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dc.contributor.authorÜNÜBOL, Nihan
dc.contributor.authorKoksalan, Kaya
dc.contributor.authorKocagoz, Tanil
dc.contributor.authorÖKTEM OKULLU, Sinem
dc.contributor.authorTÜNEY KIZILKAYA, İNCİ
dc.date.accessioned2021-03-05T14:10:05Z
dc.date.available2021-03-05T14:10:05Z
dc.date.issued2019
dc.identifier.citationÜNÜBOL N., TÜNEY KIZILKAYA İ., ÖKTEM OKULLU S., Koksalan K., Kocagoz T., "Simple Identification of Mycobacterial Species by Sequence-Specific Multiple Polymerase Chain Reactions", CURRENT MICROBIOLOGY, cilt.76, ss.791-798, 2019
dc.identifier.issn0343-8651
dc.identifier.otherav_b5ccfb36-bfb2-4354-abbf-e7ef7d7c4859
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/121016
dc.identifier.urihttps://doi.org/10.1007/s00284-019-01661-4
dc.description.abstractSeveral species of mycobacteria cause infections in humans. Species identification of clinical isolates of mycobacteria is very important for the decision of treatment and in choosing the appropriate treatment regimen. We have developed a multiplex PCR method that can identify practically all known species of mycobacteria, by determination of single-nucleotide differences at a total of 13 different polymorphic regions in the genes of rRNA and hsp65, in four PCR mixes. To achieve this goal, single-nucleotide differences in these polymorphic regions were used to divide mycobacterial species into two groups, than four, eight, etc., in an algorithmic manner. It was sufficient to reach single species level by evaluating 13 polymorphic regions. Evaluation of the multiplex PCR patterns by observable real-time electrophoresis (ORTE) simplified species identification. This new method may enable easy, rapid, and cost-effective identification of all species of mycobacteria.
dc.language.isoeng
dc.subjectMikrobiyoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.titleSimple Identification of Mycobacterial Species by Sequence-Specific Multiple Polymerase Chain Reactions
dc.typeMakale
dc.relation.journalCURRENT MICROBIOLOGY
dc.contributor.departmentAcıbadem Mehmet Ali Aydınlar Üniversitesi , Sağlık Hizmetleri Meslek Yüksekokulu ,
dc.identifier.volume76
dc.identifier.issue7
dc.identifier.startpage791
dc.identifier.endpage798
dc.contributor.firstauthorID265679


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