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Team:Rice University/Notebook/7 June 2008
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[[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 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><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 | ||
**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). | **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). | ||
Revision as of 19:13, 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
(from left to right, 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.
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