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Team:Calgary/30 July 2010
From 2010.igem.org
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[[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.]] | [[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.]] | ||
| - | [[Image:07.30.2010-ChriscpxPgel2.jpg|thumb| | + | [[Image:07.30.2010-ChriscpxPgel2.jpg|thumb|1000px|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 22:03, 30 July 2010
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.
