840:153g:Projects/project11/2010/10/07 - Revision history

Kerwin Dunham: /* Entry title */

Kerwin Dunham — Thu, 07 Oct 2010 21:03:11 GMT

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-	* ~~Insert content here~~...	+	* Tuesday we transformed bacteria with plasmids from three different parts; promoter, RBS, and double terminator. Wednesday we counted colonies on plates and innoculated media tubes for continued growth of colonies. Innoculated 3 tubes with the promoter transformed bacertia colonies, 4 tubes with the double terminator transformed bacteria colonies, and 6 tubes with the RBS transformed bacteria colonies. 6 tubes of RBS were done because of inconsistent growth on the plate.
		+	Thursday we perfomed a plasmid miniprep on all parts. Prepared glycerol stocks. Plasmids that were isolated were stored in -80C as well as the glycerol stocks.
		+	Next week we plan to digest the plasmids for our parts and run on gel to make sure the correct parts are in the plasmids.

Kerwin Dunham: Autocreate 2010/10/07 Entry for 840:153g:Projects/project11

Kerwin Dunham — Thu, 07 Oct 2010 20:56:24 GMT

Autocreate 2010/10/07 Entry for 840:153g:Projects/project11

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==Entry title==
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