Uppsala-Sweden/27 June 2011
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+ | {{Template:Uppsala-SwedenTemplate}} | ||
+ | <div class="wrap_1"> | ||
+ | <div id="mainred"> | ||
+ | <span class="hidden">Welcome to Uppsala-SwedeniEM '2011</span> | ||
+ | </div></div> | ||
+ | <div class="wrap_3"> | ||
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+ | [[Team:Uppsala-Sweden/Notebook/Brainstorming | Brainstorming ideas]] | ||
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+ | <div class="prefix_4 grid_11 suffix_1 maincontent" id="Uppsalacontent"> | ||
+ | |||
+ | |||
+ | |||
+ | == Notebook == | ||
+ | |||
+ | |||
+ | {| align="center" | ||
+ | |-valign="top" | ||
+ | |align="center" width="150pt"|{{#calendar: title=Uppsala-Sweden |year=2011 | month=06}} | ||
+ | |align="center" width="150pt"|{{#calendar: title=Uppsala-Sweden |year=2011 | month=07}} | ||
+ | |align="center" width="150pt"|{{#calendar: title=Uppsala-Sweden |year=2011 | month=08}} | ||
+ | |align="center" width="150pt"|{{#calendar: title=Uppsala-Sweden |year=2011 | month=09}} | ||
+ | |align="center" width="150pt"|{{#calendar: title=Uppsala-Sweden |year=2011 | month=10}} | ||
+ | |} | ||
+ | |||
+ | <div class="prefix_4 grid_11 suffix_1 maincontent" id="Uppsalacontent"> | ||
+ | |||
2011-06-27 | 2011-06-27 | ||
- | + | This week we started with testing the competence in our cells. For this transformation we used one positive control (plasmid pUC19 from New England Biolabs) as well as a negative control without plasmid. For the procedure we followed the protocol for transforming TOP10 competent cells. The result was good, we measured a competence efficiency of 1.7 * 10^8 transformants /ug DNA. | |
- | + | Started overnight cultures of E coli carrying the plasmids pGEM11- amilGFP (green output) and pGEM14- amilCP (blue output). For this procedure we followed the protocol Overnight culture and glycerol stock. The strains carrying the amilGFP and amilCP plasmids were provided by J.F Miller, UCLA. |
Latest revision as of 16:28, 20 July 2011
Welcome to Uppsala-SwedeniEM '2011
Notebook
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2011-06-27
This week we started with testing the competence in our cells. For this transformation we used one positive control (plasmid pUC19 from New England Biolabs) as well as a negative control without plasmid. For the procedure we followed the protocol for transforming TOP10 competent cells. The result was good, we measured a competence efficiency of 1.7 * 10^8 transformants /ug DNA.
Started overnight cultures of E coli carrying the plasmids pGEM11- amilGFP (green output) and pGEM14- amilCP (blue output). For this procedure we followed the protocol Overnight culture and glycerol stock. The strains carrying the amilGFP and amilCP plasmids were provided by J.F Miller, UCLA.