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Team:Harvard/fences/notebook
From 2010.igem.org
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| + | <td class="notebook">Week 1</td><td class="notebook"><a class="notebooklink" href="#06-14-2010">06-14-2010</a></td><td class="notebook"><a class="notebooklink" href="#06-15-2010">06-15-2010</a></td><td class="notebook"><a class="notebooklink" href="#06-16-2010">06-16-2010</a></td><td class="notebook"><a href="#06-17-2010">06-17-2010</a></td><td class="notebook"><a class="notebooklink" href="#06-18-2010">06-18-2010</a></td> | ||
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==06-15-2010 [ [[#top|top]] ]== | ==06-15-2010 [ [[#top|top]] ]== | ||
Revision as of 18:56, 23 October 2010
notebook calendar
06-14-2010 [ top ]
LacI Transformation
Performed bacterial transformation according to Silver:_Bacterial_Transformation, however we used 1μL in step 3, and used entire tube of TOP10 competent cells instead of only 10-15μL.
Transformed the following, each into its own tube of TOP10 E.Coli:
1) LacI with a rapid degredation tail attached, biobrick BBa_C0012, located on plate 1, well 2O, plasmid pSB1A2
2) LacI wildtype, biobrick BBa_I732100, located on plate 2, well 10E, plasmid pSB1A3
Streaked 100μL each of 1 and 2 onto separate LB + Amp dishes, along with a control dish of 100μL untransformed TOP10 E.Coli cells.
Plates incubated overnight, colonies observed in all plates except the control.
