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https://repository.seku.ac.ke/handle/123456789/260Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Muluvi, Geoffrey M. | - |
| dc.contributor.author | Machuka, Jesse | - |
| dc.contributor.author | Njagi, W. | - |
| dc.contributor.author | Gichuki, S. T. | - |
| dc.contributor.author | Macharia, C. | - |
| dc.date.accessioned | 2014-12-01T08:36:07Z | - |
| dc.date.available | 2014-12-01T08:36:07Z | - |
| dc.date.issued | 2010 | - |
| dc.identifier.citation | Proceedings of the 10th KARI biennial scientific conference | en_US |
| dc.identifier.uri | http://ir-library.ku.ac.ke/handle/123456789/10403 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/260 | - |
| dc.description.abstract | An 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.iso | en | en_US |
| dc.title | Optimisation of parameters for agrobacterium-mediated transformation of sweet potato | en_US |
| dc.type | Presentation | en_US |
| Appears in Collections: | School of Science and Computing (CS) | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Muluvi_Optimisation of parameters for agrobacterium-mediated transformation of sweet potato.pdf | Abstract | 4.33 kB | Adobe PDF | ![]() View/Open |
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