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dc.contributor.authorPeck, Ken_US
dc.contributor.authorWung, SLen_US
dc.contributor.authorChang, GSen_US
dc.contributor.authorYen, JJYen_US
dc.contributor.authorHsieh, YZen_US
dc.date.accessioned2014-12-08T15:01:52Z-
dc.date.available2014-12-08T15:01:52Z-
dc.date.issued1997-04-01en_US
dc.identifier.issn0003-2700en_US
dc.identifier.urihttp://hdl.handle.net/11536/617-
dc.description.abstractRestriction mapping is one of the essential steps in gene analysis and molecular biology studies, Slab gel electrophoresis is the traditional way to separate DNA fragments for restriction mapping, However, slab gel electrophoresis does not provide sufficient resolution as required in many mapping applications, and the use of radioisotopes in traditional mapping methods creates health hazards, In the present study, capillary electrophoresis coupled with laser-induced fluorescence detection and a modified partial digestion mapping procedure was developed to map DNA fragments. By using capillary electrophoresis, a restriction map of a genomic lambda phage clone of human interleukin 5 receptor a chain (IL5R alpha) gene was constructed, The IL5R alpha gene was analyzed to have five XbaI enzyme cutting sites at locations 1370, 2290, 2950, 5430, and 9330, The system was further characterized by using pBluescript SK(+) phagemid DNA as a model, Using a sequence-derived map as a reference, the pBluescript SK(+) restriction map constructed by capillary electrophoresis had an accuracy greater than 90%.en_US
dc.language.isoen_USen_US
dc.titleRestriction mapping of genes by capillary electrophoresis with laser-induced fluorescence detectionen_US
dc.typeArticleen_US
dc.identifier.journalANALYTICAL CHEMISTRYen_US
dc.citation.volume69en_US
dc.citation.issue7en_US
dc.citation.spage1380en_US
dc.citation.epage1384en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1997WQ77700024-
dc.citation.woscount11-
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