نمایش مختصر رکورد

dc.contributor.authorSekhavati, Mohammad Hadien_US
dc.contributor.authorTahmoorespur, Mojtabaen_US
dc.contributor.authorJafarpour, Farnooshen_US
dc.contributor.authorDormiani, Kianoushen_US
dc.contributor.authorKhazaie, Yahyaen_US
dc.contributor.authorGhaedi, Kamranen_US
dc.contributor.authorHosseini, Sayyed Mortezaen_US
dc.contributor.authorForouzanfar, Mahboobehen_US
dc.contributor.authorNasr Esfahani, Mohammad Hosseinen_US
dc.date.accessioned1399-07-08T20:19:10Zfa_IR
dc.date.accessioned2020-09-29T20:19:10Z
dc.date.available1399-07-08T20:19:10Zfa_IR
dc.date.available2020-09-29T20:19:10Z
dc.date.issued2014-12-01en_US
dc.date.issued1393-09-10fa_IR
dc.date.submitted2013-07-29en_US
dc.date.submitted1392-05-07fa_IR
dc.identifier.citationSekhavati, Mohammad Hadi, Tahmoorespur, Mojtaba, Jafarpour, Farnoosh, Dormiani, Kianoush, Khazaie, Yahya, Ghaedi, Kamran, Hosseini, Sayyed Morteza, Forouzanfar, Mahboobeh, Nasr Esfahani, Mohammad Hossein. (2014). Identification of a Specific Pseudo attP Site for Phage PhiC31 Integrase in Bovine Genome. Iranian Journal of Biotechnology, 12(4), 1-9. doi: 10.15171/ijb.1013en_US
dc.identifier.issn1728-3043
dc.identifier.issn2322-2921
dc.identifier.urihttps://dx.doi.org/10.15171/ijb.1013
dc.identifier.urihttp://www.ijbiotech.com/article_7571.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/85762
dc.description.abstractBackground: PhiC31 integrase system provides a new platform in various felid of research, mainly in gene therapy and creation of transgenic animals. This system enables integration of exogenous DNA into preferred locations in mammalian genomes, which results in robust, long-term expression of the integrated transgene. Objectives: Identification of a novel pseudo attP site. Materials and Methods: Genomic DNA was extracted from primary bovine fetal fibroblast cells, which were stably transfected with EGFP and phiC31 integrase cDNAs carrying vectors. An inverse PCR was carried out for production of mini-circle DNAs and followed by sequencing. Results: A new specific pseudo attP site termed BF5 was identified in bovine genome.  This site is located in an intergenic AT rich region on chromosome 5 with similar features of other mammalian attP pseudo sites.  Furthermore, direct sequencing of generated attL site confirmed that site-specific transgene recombination was occurred at this site. Conclusions: This finding confirmed that phiC31 integrase could be feasible for production of transgenic animals for biotechnological applications.en_US
dc.format.extent785
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherNational Institute of Genetic Engineering and Biotechnologyen_US
dc.relation.ispartofIranian Journal of Biotechnologyen_US
dc.relation.isversionofhttps://dx.doi.org/10.15171/ijb.1013
dc.subjectPhiC31 intagraseen_US
dc.subjectPseudo attP siteen_US
dc.subjectProtein expressionen_US
dc.subjectRecombinationen_US
dc.titleIdentification of a Specific Pseudo attP Site for Phage PhiC31 Integrase in Bovine Genomeen_US
dc.typeTexten_US
dc.typeResearch Paperen_US
dc.contributor.departmentDepartment of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iranen_US
dc.contributor.departmentDepartment of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, I.R. IRANen_US
dc.contributor.departmentDepartment of Reproduction and Development at Reproductive Biomedicine Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRANen_US
dc.contributor.departmentDepartment of Molecular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRANen_US
dc.contributor.departmentDepartment of Molecular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRANen_US
dc.contributor.departmentDepartment of Biology, School of Sciences, University of Isfahan & Department of Cellular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnologyen_US
dc.contributor.departmentDepartment of Reproduction and Development at Reproductive Biomedicine Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRANen_US
dc.contributor.departmentDepartment of Molecular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRANen_US
dc.contributor.departmentDepartment of Molecular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRANen_US
dc.citation.volume12
dc.citation.issue4
dc.citation.spage1
dc.citation.epage9


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