Edinburgh/13 July 2008
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* Signs of growth on ''Cellulomonas'' plates 28 and 29. | * Signs of growth on ''Cellulomonas'' plates 28 and 29. | ||
* Minipreps '''M25 to M30''' of possible rbs+''dxs'' clones from plate 34. | * Minipreps '''M25 to M30''' of possible rbs+''dxs'' clones from plate 34. | ||
- | * PCR '''P12''' to obtain rbs+''dxs'' fusion product in case minipreps didn't work. Template was ligation L11, and primers were rbs2clonf1 and pSB1A2insr1. Annealing was 58°C, extension 40s using KOD.<br /> | + | * PCR '''P12''' to obtain rbs+''dxs'' fusion product in case minipreps didn't work. Template was ligation L11, and primers were rbs2clonf1 and pSB1A2insr1. Annealing was 58°C, extension 40s using KOD. |
+ | * M25 to M30 were digested with SacI/SpeI and run on '''gel 12''' along with undigested P12. This shows that M25 to M30 are no good.<br /> | ||
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:::: '''[[Edinburgh/14_July_2008|Next Entry >]]''' | :::: '''[[Edinburgh/14_July_2008|Next Entry >]]''' |
Revision as of 15:21, 21 August 2008
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Week 4
Sunday 13 July 08
- Signs of growth on Cellulomonas plates 28 and 29.
- Minipreps M25 to M30 of possible rbs+dxs clones from plate 34.
- PCR P12 to obtain rbs+dxs fusion product in case minipreps didn't work. Template was ligation L11, and primers were rbs2clonf1 and pSB1A2insr1. Annealing was 58°C, extension 40s using KOD.
- M25 to M30 were digested with SacI/SpeI and run on gel 12 along with undigested P12. This shows that M25 to M30 are no good.