2010.igem.org/Team:Harvard/fences/notebook

From 2010.igem.org

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{{HarvardFancybox}}
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Our lab notebook on OpenWetWare can be found [http://openwetware.org/wiki/IGEM:Harvard/2009/Notebook/Harvard_iGEM_2010 here].
Our lab notebook on OpenWetWare can be found [http://openwetware.org/wiki/IGEM:Harvard/2009/Notebook/Harvard_iGEM_2010 here].
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==June 14 2010==
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<b>LacI Transformation</b>
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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.
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Transformed the following, each into its own tube of TOP10 E.Coli:
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1) LacI with a rapid degredation tail attached, biobrick BBa_C0012, located on plate 1, well 2O, plasmid pSB1A2
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2) LacI wildtype, biobrick BBa_I732100, located on plate 2, well 10E, plasmid pSB1A3
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Streaked 100μL each of 1 and 2 onto separate LB + Amp dishes, along with a control dish of 100μL untransformed TOP10 E.Coli cells.
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Plates incubated overnight, colonies observed in all plates except the control.

Latest revision as of 16:29, 10 October 2010


Our lab notebook on OpenWetWare can be found here.


June 14 2010

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.