Team:Rice University/Notebook/7 June 2008

From 2008.igem.org

(Difference between revisions)
 
Line 4: Line 4:
**Prepared gel electrophoresis of above digest along with solution of lambda DNA with 1Kb standard
**Prepared gel electrophoresis of above digest along with solution of lambda DNA with 1Kb standard
[[Image:20080607_gel.jpg|100px|left]]
[[Image:20080607_gel.jpg|100px|left]]
-
(from left to right, lane 1: 1Kb, lane 2: lambda DNA, lane 3: lambda with XhoI)
+
(from right to left, 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><BR><BR><BR><BR>
<BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR><BR>
*Taylor Stevenson
*Taylor Stevenson

Latest revision as of 19:15, 25 June 2008

Saturday 7 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
20080607 gel.jpg

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

















  • Taylor Stevenson
    • Phage infected XL1-blue MR colonies cultured in 96 deep-well plate were spotted onto two EMB plates using a 2uL plate replicator. Both plates were incubated O/N, one at 30*C and one at 42*C (temp is high enough to denature the CI repressor, causing any lysogen to become lytic).
    • Result-both plates showed no bacterial growth after 24h.





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