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Team:Calgary/30 July 2010
From 2010.igem.org
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'''Friday July 30, 2010''' | '''Friday July 30, 2010''' | ||
| - | [[Image:07.30.2010-ChriscpxPgel.jpg|thumb|400px|Chris's first gel of the attempted gradient PCR to remove the CpxP promoter from the E. coli genome. This line of tubes | + | [[Image:07.30.2010-ChriscpxPgel.jpg|thumb|400px|Chris's first gel of the attempted gradient PCR to remove the CpxP promoter from the E. coli genome. This line of tubes ran from 50°C to 56°C and at a MgCl<sub>2</sub> concentration of 1.5 µM.]] |
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| + | [[Image:07.30.2010-ChriscpxPgel2.jpg|thumb|400px|Chris's second gel of the attempted gradient PCR to remove the CpxP promoter from the E. coli genome. This line of tubes ran from 50°C to 56°C and at a MgCl<sub>2</sub> concentration of 2.0 µM.]] | ||
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Revision as of 22:02, 30 July 2010
Notebook
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Friday July 30, 2010
Chris's first gel of the attempted gradient PCR to remove the CpxP promoter from the E. coli genome. This line of tubes ran from 50°C to 56°C and at a MgCl2 concentration of 1.5 µM.
Chris's second gel of the attempted gradient PCR to remove the CpxP promoter from the E. coli genome. This line of tubes ran from 50°C to 56°C and at a MgCl2 concentration of 2.0 µM.
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