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Team:Rice University/Notebook/7 June 2008
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(New page: =Saturday 7 June= *Selim Sheikh: **Prepare digestion of lambda DNA with XhoI only **Prepare gel electrophoresis of above digest along with solution of lambda DNA with 1Kb standard [[Image:...) |
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=Saturday 7 June= | =Saturday 7 June= | ||
*Selim Sheikh: | *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 |
[[Image:20080607_gel.jpg|100px|left]] | [[Image:20080607_gel.jpg|100px|left]] | ||
| - | (from | + | (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> | ||
| + | *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. | ||
| + | <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]] | ||
| + | |} | ||
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
(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.
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