Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/60122
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dc.contributor.authorC. Nontaswatsrien_US
dc.contributor.authorS. Fukaien_US
dc.contributor.authorS. Ruamrungsrien_US
dc.date.accessioned2018-09-10T03:38:21Z-
dc.date.available2018-09-10T03:38:21Z-
dc.date.issued2008-01-01en_US
dc.identifier.issn05677572en_US
dc.identifier.other2-s2.0-61449165028en_US
dc.identifier.other10.17660/ActaHortic.2008.788.12en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=61449165028&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/60122-
dc.description.abstractAnthers of Dianthus chinensis L. and D. barbatus L. containing microspores at the tetrad, uninucleate or binucleate stage were cultured on various combinations of media and growth regulators. The callus induction of D. chinensis were high when cultured on MS medium containing 1 mg L-12,4-D + 0.1 mg L-1NAA and shoot regeneration of D. chinensis were high when cultured on B5 containing 1 mg L-1TDZ + 0.1 mg L-1NAA. Anther culture of D. barbatus in MS or B5 medium containing 1 mg L-1TDZ and 0.1 mg L-1NAA produced highest percentage of calli. Nevertheless only calli from anther cultured on MS medium containing 1 mg L-1TDZ and 0.1 mg L-1NAA could produce shoots. The ploidy levels of most regenerated shoots, determined by flow-cytometry, were diploid.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleCallus induction and plant regeneration of Dianthus chinensis L. and Dianthus barbatus L. via Anther cultureen_US
dc.typeBook Seriesen_US
article.title.sourcetitleActa Horticulturaeen_US
article.volume788en_US
article.stream.affiliationsMaejo Universityen_US
article.stream.affiliationsKagawa Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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