Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/5884
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dc.contributor.authorMuthukumar, B-
dc.contributor.authorArockiasamy, D I-
dc.contributor.authorNatarajan, E-
dc.date.accessioned2009-08-12T05:29:13Z-
dc.date.available2009-08-12T05:29:13Z-
dc.date.issued2004-07-
dc.identifier.issn0975-0967 (Online); 0972-5849 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/5884-
dc.description449-451en_US
dc.description.abstractIn vitro plant regeneration was achieved in Datura metel from nodal explants collected from both in vitro germinated seedlings and field grown plants (in vivo). The explants were cultured on MS medium with BAP (0.5-3.0 mg/l) and NAA (0.5 mg/l). The nodal explants isolated from in vivo source exhibited a greater number of healthy multiple shoots than in vitro. BAP at 3 mg/l with NAA at 0.5 mg/l was found to be optimal for regeneration of shootlets.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl.7 A 01 H 4/00, 5/00en_US
dc.sourceIJBT Vol.3(3) [July 2004]en_US
dc.subjectDatura metelen_US
dc.subjectmedicinalen_US
dc.subjectin vitro regenerationen_US
dc.subjectnodal explantsen_US
dc.subjectBAPen_US
dc.subjectorganogenesisen_US
dc.titleDirect organogenesis in Datura metel L. from in vitro and in vivo nodal explantsen_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.03(3) [July 2004]

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