IGEM:Harvard/2009/Notebook/Harvard iGEM 2010/2010/06/14: Difference between revisions
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== | ==Team Flavor== | ||
* | * Miraculin and brazzein constructs due to arrive on Wednesday from Mr. Gene | ||
===BioBrick Transformation=== | |||
BioBrick parts from the 2010 iGEM kit were transformed and grown in highly competent TURBO bacteria. <br> | |||
*Wintergreen Scent Pathway: <br> | |||
BBa_J45700 - entire pathway, Ampicillin <br> | |||
BBa_J45004 - BSMT1 only, Ampicillin <br> | |||
(Not in 2010 BB Kit: BBa_J45017 - PchB, PchA) <br> | |||
*Banana Scent Pathway: <br> | |||
BBa_J45250 - ATF3 + Promoter, Ampicillin?<br> | |||
BBa_J45014 - ATF3 only, Ampicillin <br> | |||
(Not in BB 2010 Kit: BBa_J45400 - BAT2 and THI3)<br> | |||
==Team Fence== | |||
<b>LacI Transformation</b> | |||
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. | |||
[[Image:Colonies 6-15-10.jpg|300px]] | |||
[[Image:Colonies-2 6-15-10.jpg|300px]] | |||
[[Image:Colonies-3 6-15-10.jpg|300px]] | |||
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Revision as of 15:31, 18 June 2010
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Team Flavor
BioBrick TransformationBioBrick parts from the 2010 iGEM kit were transformed and grown in highly competent TURBO bacteria.
BBa_J45700 - entire pathway, Ampicillin
BBa_J45250 - ATF3 + Promoter, Ampicillin? Team FenceLacI 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.
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