Team:Calgary/30 July 2010

From 2010.igem.org

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'''Friday July 30, 2010'''
'''Friday July 30, 2010'''
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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 rawn from 50&deg;C to 56&deg;C and at a MgCl<sub>2</sub> concentration of 1 &micro;M.]]
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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&deg;C to 56&deg;C and at a MgCl<sub>2</sub> concentration of 1.5 &micro;M.]]
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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&deg;C to 56&deg;C and at a MgCl<sub>2</sub> concentration of 2.0 &micro;M.]]
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Revision as of 22:02, 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.


No notebook page exists for this date. Sorry!