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dc.contributor.authorD. Joshien_US
dc.contributor.authorM. H. Parken_US
dc.contributor.authorA. Saeungen_US
dc.contributor.authorW. Choochoteen_US
dc.contributor.authorG. S. Minen_US
dc.date.accessioned2018-09-04T04:41:11Z-
dc.date.available2018-09-04T04:41:11Z-
dc.date.issued2010-07-01en_US
dc.identifier.issn17550998en_US
dc.identifier.issn1755098Xen_US
dc.identifier.other2-s2.0-77954749255en_US
dc.identifier.other10.1111/j.1755-0998.2010.02835.xen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77954749255&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50452-
dc.description.abstractFollowing the recent emergence of malaria in South Korea, vector control has been an important task. For this, vector identification is very important. Earlier, two PCR-based assays have been described. But, poor species resolution and their ability to include only 4-5 species limit their use. Thus, it has now become important to revise the assay identifying these members. In this study, a new assay based on internal transcribed spacer 2 and 28S of ribosomal DNA has been described. The assay successfully identified all the Korean malaria vector mosquitoes. Therefore, it is an indispensable tool to study ecology, abundance and biology of these species. © 2010 Blackwell Publishing Ltd.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleMultiplex assay to identify Korean vectors of malariaen_US
dc.typeJournalen_US
article.title.sourcetitleMolecular Ecology Resourcesen_US
article.volume10en_US
article.stream.affiliationsInha University, Incheonen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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