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Team:Leicester/August2012
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<h3 class="calendar"> Wednesday 1st August 2012</h3> | <h3 class="calendar"> Wednesday 1st August 2012</h3> | ||
<div class="day"> | <div class="day"> | ||
| - | + | <p>(9:30 am) Several members of the team are given wrong start times, so only 1 student arrived in the lab at 9:30, however with the work needed to be done all the rest of the team are quickly on their way.</p> | |
| + | <p>(10:00 am) Today the team is going to start creating a DNA library of the ''Pseudomonas. sp'' so that once the NB26 strain arrives it can be compared straight away to give an idea which genes could be involved in the degredation of polystyrene and to help start narrowing our search.</p> | ||
| + | <p> The team starts by creating the control plates with ''E. coli''. The 3 plates created are: plain mineral media, and two of the minimal media with 5% polystyrene sprinkled on top. The ''E. coli'' is being plated on the plain media as well as one of the polystyrene sprinkled plates.</p> | ||
</div> | </div> | ||
Revision as of 09:01, 1 August 2012
Wednesday 1st August 2012
(9:30 am) Several members of the team are given wrong start times, so only 1 student arrived in the lab at 9:30, however with the work needed to be done all the rest of the team are quickly on their way.
(10:00 am) Today the team is going to start creating a DNA library of the ''Pseudomonas. sp'' so that once the NB26 strain arrives it can be compared straight away to give an idea which genes could be involved in the degredation of polystyrene and to help start narrowing our search.
The team starts by creating the control plates with ''E. coli''. The 3 plates created are: plain mineral media, and two of the minimal media with 5% polystyrene sprinkled on top. The ''E. coli'' is being plated on the plain media as well as one of the polystyrene sprinkled plates.
