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Team:TUDelft/19 August 2009
From 2009.igem.org
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{| border="1" align="center" | {| border="1" align="center" | ||
| - | | | + | | lane || Part || Expected Plasmid Size || Status |
|- align="center" | |- align="center" | ||
| 1 || [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder] || 2953 || | | 1 || [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder] || 2953 || | ||
|- align="center" | |- align="center" | ||
| - | | 2 || | + | | 2 || !Fr1n upstream || 1162 || ok |
|- align="center" | |- align="center" | ||
| - | | 3 || | + | | 3 || !Fr1n downstream || 311 || ok |
| + | |- align="center" | ||
| + | | 4 || destination plasmid || 1162 || ok | ||
|} | |} | ||
{{Template:TUDelftiGEM2009_end}} | {{Template:TUDelftiGEM2009_end}} | ||
Revision as of 13:37, 28 August 2009
Lab Notebook
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19 August 2009
Tim Weenink
After yesterdays horrible discovery that the I-SceI Homing Endonuclease we got from MIT was actually T4 DNA ligase we had to adjust our cloning strategy. The more primitive part without promoter was found to be the correct one, except that is was assembled with part !A instead of p(LacI). So we did that assembly again today. With p(LacI) from the delay team upstream, *T1 (downstream) and backbone pSB1C3 (also from the delay team). Both RbCl chemically comp and EC electrocomp cells were transformed.
Saeed
| lane | Part | Expected Plasmid Size | Status |
| 1 | [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder] | 2953 | |
| 2 | !Fr1n upstream | 1162 | ok |
| 3 | !Fr1n downstream | 311 | ok |
| 4 | destination plasmid | 1162 | ok |
