Template:Team:SydneyUni Australia/Calendar/Events List

From 2013.igem.org

(Difference between revisions)
Line 28: Line 28:
start: new Date(2013, 4, 17),
start: new Date(2013, 4, 17),
description: '<b>Members:</b> Coleman, Viv, Desmond, Rob and Hugh <br> <b>What we did: </b> We made some solutions of LB, LB agar and TE. We staked out our claim in the lab. Yay!'
description: '<b>Members:</b> Coleman, Viv, Desmond, Rob and Hugh <br> <b>What we did: </b> We made some solutions of LB, LB agar and TE. We staked out our claim in the lab. Yay!'
-
},
 
-
{
 
-
title: 'Meeting',
 
-
start: new Date(2013, 4, 17),
 
-
description: '<b>Members:</b> Rob <br> <b>What we did: Robbie introduces iGEM to the Manager of Inspiring Australia in NSW, facilitator for National Science Week. Advice'
 
},
},
{
{
Line 66: Line 61:
},
},
// -----------------Week 3 ----------------
// -----------------Week 3 ----------------
-
{
+
{
 +
title: 'Meeting with Yagiz',
 +
start: new Date(2013, 5, 3),
 +
description: '<b>Members:</b> Nick, Rob, Andrew, Viv, Shuravi, Cyril, Desmond, Hugh, Evelyn <br> <b>What we did: </b>Met with Yagiz and Rob from the MQ univeristy iGEM team for a general introduction to iGEM and some helpful advice. '
 +
},
 +
{
 +
title: 'Lab induction',
 +
start: new Date(2013, 5, 3),
 +
description: '<b>Members:</b> Nick, Rob, Andrew, Viv, Shuravi, Cyril, Desmond, Hugh <br> <b>What we did: </b>Lab induction and safety brief.  '
 +
},
 +
{
title: 'PCR analysis and GC analysis of DCA metabolism',
title: 'PCR analysis and GC analysis of DCA metabolism',
start: new Date(2013, 5, 3),
start: new Date(2013, 5, 3),
-
description: '<b>Members:</b> Colman, Hugh, Rob <br> <b>What we did: </b> We ran a gel of last Friday’s PCR. The PCR was of pBS(ToMO) extracted from Wood’s E. Coli TG1, with primers iGEM 1 & 2. The banding on the gel was obscure, potentially due to too much template and could not be used. <br><br> We used the Gas Chromatographer (GC) to look at our two DCA treatments of E. Coli (transformed with either pBBR or pBS(ToMO)). Both had pretty much the same reading but it is uncertain yet whether this is because pBS(ToMO) was lost or altered during the extended incubation from Week 2, or whether ToMO was unable to degrade DCA. We also set up standardised solutions of NaCl in KP buffer for a future Cl assay.'
+
description: '<b>Members:</b> Coleman, Hugh, Rob <br> <b>What we did: </b> We ran a gel of last Friday’s PCR. The PCR was of pBS(ToMO) extracted from Wood’s E. Coli TG1, with primers iGEM 1 & 2. The banding on the gel was obscure, potentially due to too much template and could not be used. <br><br> We used the Gas Chromatographer (GC) to look at our two DCA treatments of E. Coli (transformed with either pBBR or pBS(ToMO)). Both had pretty much the same reading but it is uncertain yet whether this is because pBS(ToMO) was lost or altered during the extended incubation from Week 2, or whether ToMO was unable to degrade DCA. We also set up standardised solutions of NaCl in KP buffer for a future Cl assay.'
},
},
// -----------------Week 4 ----------------
// -----------------Week 4 ----------------
-
{
+
{
 +
title: 'Primer tutorial',
 +
start: new Date(2013, 5, 14),
 +
description: '<b>Members:</b> Nick, Rob, Andrew, Viv, Shuravi, Desmond <br> <b>What we did: </b> We went over possible primer design considerations for the project. '
 +
},
 +
{
title: 'Redo of ToMO Trial',
title: 'Redo of ToMO Trial',
start: new Date(2013, 5, 22),
start: new Date(2013, 5, 22),

Revision as of 03:10, 28 September 2013

Retrieved from "http://2013.igem.org/Template:Team:SydneyUni_Australia/Calendar/Events_List"