Revision as of 19:21, 25 June 2008

Tuesday 10 June

Selim Sheikh:
- Prepared digestion of lambda DNA with XhoI only
- Prepared gel electrophoresis of above digest along with solution of lambda DNA with 1Kb standard

(from left to right, lane 1: 1Kb, lane 2: lambda DNA, lane 3: lambda with XhoI)

Taylor Stevenson
- Phage infected XL1-Blue MR colonies were picked and used used to innoculate a 96 deep-well plate containing 1.0mL of LB in each well.
- innoculated 96 deep-well plate was cultured O/N @ 30*C shaking @ 250 rpm.

Home	The Team	The Project	Parts Submitted to the Registry	Modeling	Notebook

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 [[Image:20080610_gel.jpg|100px|left]]
 (from left to right, lane 1: 1Kb, lane 2: lambda DNA, lane 3: lambda with XhoI)
+<BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR>
+*Taylor Stevenson
+**Phage infected XL1-Blue MR colonies were picked and used used to innoculate a 96 deep-well plate containing 1.0mL of LB in each well.
+**innoculated 96 deep-well plate was cultured O/N @ 30*C shaking @ 250 rpm.
+<BR><BR><BR><BR>
+{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
+!align="center"|[[Team:Rice_University|Home]]
+!align="center"|[[Team:Rice_University/Team|The Team]]
+!align="center"|[[Team:Rice_University/Project|The Project]]
+!align="center"|[[Team:Rice_University/Parts|Parts Submitted to the Registry]]
+!align="center"|[[Team:Rice_University/Modeling|Modeling]]
+!align="center"|[[Team:Rice_University/Notebook|Notebook]]
+|}