Please use this identifier to cite or link to this item: https://repository.seku.ac.ke/handle/123456789/260
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dc.contributor.authorMuluvi, Geoffrey M.-
dc.contributor.authorMachuka, Jesse-
dc.contributor.authorNjagi, W.-
dc.contributor.authorGichuki, S. T.-
dc.contributor.authorMacharia, C.-
dc.date.accessioned2014-12-01T08:36:07Z-
dc.date.available2014-12-01T08:36:07Z-
dc.date.issued2010-
dc.identifier.citationProceedings of the 10th KARI biennial scientific conferenceen_US
dc.identifier.urihttp://ir-library.ku.ac.ke/handle/123456789/10403-
dc.identifier.urihttp://hdl.handle.net/123456789/260-
dc.description.abstractAn Agrobacterium-mediated transformation and somatic regeneration protocol was adapted for a Kenyan sweet potato variety, KSP36. A model cultivar, CTP560 was used as a control. For selection of transformed explants paramomycin was found to be effective at 25mg/L while kanamycin was effective at 20mg/L. The lower concentrations of 2,4-dichlorophenoxyacetic acid (2,4-D) concentrations proved better for regeneration as opposed to the higher 2,4-D concentrations. Zeatin/ IAA (indole acetic acid) was more effective at embryo production as opposed to kinetin/ 2,4-D medium in both cultivars. Out of the 18 KSP36 plants tested by PCR, 11 tested positive for the coat protein gene while 9 out of the 19 CPT560 plants tested positive. This protocol can be recommended for other sweet potato varieties.en_US
dc.language.isoenen_US
dc.titleOptimisation of parameters for agrobacterium-mediated transformation of sweet potatoen_US
dc.typePresentationen_US
Appears in Collections:School of Science and Computing (CS)

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