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dc.creatorDmitrović, Slavica
dc.creatorMitrović, Aleksandra
dc.creatorĆulafić, Ljubinka
dc.date.accessioned2017-11-23T11:15:19Z
dc.date.available2015-11-17T10:26:51Z
dc.date.issued2005sr
dc.identifier.issn0006-3134sr
dc.identifier.otherRad_konverzija_3699sr
dc.identifier.urihttps://radar.ibiss.bg.ac.rs/handle/123456789/1704
dc.description.abstractIn order to establish an efficient system for in vitro plant regeneration of a short day plant Chenopodium rubrum L. and a long day plant Chenopodium murale L., optimum culture conditions for somatic embryogenesis were investigated. The effects of different growth regulators, their combination and their concentrations on somatic embryos induction in different explant types (root, hypocotyl, cotyledon and leaf) were tested. Somatic embryogenesis was induced in both plants on Murashige and Skoog (MS) medium supplemented with sucrose (3%), agar (0.7%) and 1-10 mu M 2,4-dichlorophenoxyacetic acid (2,4-D) as the sole growth regulator. The largest embryogenic capacity was found in root explants of Chenopodium rubrum on 1 mu M 2,4-D and in basal parts of cotyledons in C. murale plants on 10 mu M 2,4-D.en
dc.description.sponsorshipnullsr
dc.language.isoEnglishsr
dc.rightsrestrictedAccess
dc.sourceBiologia Plantarumsr
dc.titleSomatic embryogenesis in Chenopodium rubrum and Chenopodium murale in vitroen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractЋулафић, Љубинка; Митровић, Aлександра; Миливојевић, Славица С;
dc.citation.issue1sr
dc.citation.volume49sr
dc.identifier.doi10.1007/s00000-005-5039-5
dc.identifier.scopus2-s2.0-17044392717
dc.identifier.wos000227744000006
dc.citation.spage35
dc.citation.epage39sr
dc.type.versionpublishedVersionen
dc.citation.rankM22
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_ibiss_1704


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