840:153g:Projects/project11/2010/11/18 - Revision history

Derek Blanchard: /* Entry title */

Derek Blanchard — Thu, 18 Nov 2010 21:33:25 GMT

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		+	Tuesday: We digested our 9 remaining colonies yet to be screened for our (gene&double terminator)superpart and ran on a gel. results from this gel of the 9 remaining colonies resembled that from previous gels we ran. Base pair length ended up between 100-200bp so we believe there is a problem with the Ecor1 during the ligation process preventing our two parts break apart correctly in order to ligate them together.

		+	We also religated our left over Gene & double terminator parts that we had stored. In preperation for another bacteria transformation.
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		+	Thursday: transformed bacteria with our newly religated gene & double terminator superpart. In preperation for a digestion and gel electrophoresis.

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Derek Blanchard: Autocreate 2010/11/18 Entry for 840:153g:Projects/project11

Derek Blanchard — Thu, 18 Nov 2010 21:25:02 GMT

Autocreate 2010/11/18 Entry for 840:153g:Projects/project11

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