Template:Team:SydneyUni Australia/Calendar/Events List

(Difference between revisions)

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 					start: new Date(2013, 9, 23),
 					description: '<b>Members:</b> Rob, Hugh, Andrew <br> <b>What we did: </b> Patching and lysing cells from transformation plates for PCR screen and pH-chloroacetate screens. No efficient cloning for whole pathway, only for individual parts with tetR-inducible promoter system. Set-up chloride assay for degradation of DCA by clones containing tetR-p450 and tetR-aldA-dhlB-dhlA.'
-				},
-				{
-					title: 'Chloride assay',
-					start: new Date(2013, 9, 24),
-					description: '<b>Members:</b> Rob, Andrew <br> <b>What we did: </b> Performed chloride assay. Appears there is reasonable degradation of DCA by p450.
-'
-				},
-				{
-					title: 'Acetaldehyde growth inhibition',
-					start: new Date(2013, 9, 25),
-					description: '<b>Members:</b> Rob, Andrew <br> <b>What we did: </b> Set-up an experiment to confirm aldA expression through growth inhibition of control E. coli in LB-acetaldehyde.'
-				},
-				{
-					title: 'Characterising new parts',
-					start: new Date(2013, 9, 26),
-					description: '<b>Members:</b> Rob, Andrew <br> <b>What we did: </b> Another LB-acetaldehyde growth experiment in triplicate with a promising tetR-aldA clone. Incubated tetR-p450 clones with DCA in triplicate to confirm result from the 24th October, after 6 hours incubation, GC was not promising. Set-up an ethene-epoxide assay to confirm p450 expression. '
 				}
 			]

Revision as of 04:57, 28 October 2013