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Edinburgh/8 July 2008
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| - | * New primers for ''crt'' BioBricks arrived. Performed PCR with KOD using primer pairs crtBf2 (new) + crtBr2 (old)('''P8'''), crtIf2 + crtIr2 (both new) ('''P9'''), and crtYf2 (new) + crtYr2 (old)('''P10'''). The template for P8 and P10 was a suspension of ''Pantoea ananatis'' cells from plate 17; for P9, Douglas's maxiprep DNA from 19 Feb (with the PstI sites mutated out) was used. In all cases annealing was at | + | </style> |
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| + | |align="left" width="150pt"|{{#calendar: title=Edinburgh |year=2008 | month=08}} | ||
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| + | :::: '''[[Edinburgh/7_July_2008|< Previous Entry]]''' | ||
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| + | == Week 4 == | ||
| + | === Tuesday 8 July 08 === | ||
| + | |||
| + | * New primers for ''crt'' BioBricks arrived. Performed PCR with KOD using primer pairs crtBf2 (new) + crtBr2 (old)('''P8'''), crtIf2 + crtIr2 (both new) ('''P9'''), and crtYf2 (new) + crtYr2 (old)('''P10'''). The template for P8 and P10 was a suspension of ''Pantoea ananatis'' cells from plate 17; for P9, Douglas's maxiprep DNA from 19 Feb (with the PstI sites mutated out) was used. In all cases annealing was at 55°C and extension for 30s. '''Gel 9''' showed that P8 and P9 had worked, with pure products of the expected size seen, but no product was seen for P10. | ||
* ''glgC'' mutagenesis: Transformed competent cells with ligation products L6 and L7; plated cells on '''Plates 22 and 23''' (L6) and '''Plates 24 and 25''' (L7). | * ''glgC'' mutagenesis: Transformed competent cells with ligation products L6 and L7; plated cells on '''Plates 22 and 23''' (L6) and '''Plates 24 and 25''' (L7). | ||
| - | * ' | + | * Ran '''gel 9''' to check size of X1 (J33201) and X2 (pSB1A2+''dxs'') HindIII restriction digest. The digest looked fine.<br /> |
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| + | :::: '''[[Edinburgh/9_July_2008|Next Entry >]]''' | ||
Revision as of 11:48, 21 August 2008
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Week 4
Tuesday 8 July 08
- New primers for crt BioBricks arrived. Performed PCR with KOD using primer pairs crtBf2 (new) + crtBr2 (old)(P8), crtIf2 + crtIr2 (both new) (P9), and crtYf2 (new) + crtYr2 (old)(P10). The template for P8 and P10 was a suspension of Pantoea ananatis cells from plate 17; for P9, Douglas's maxiprep DNA from 19 Feb (with the PstI sites mutated out) was used. In all cases annealing was at 55°C and extension for 30s. Gel 9 showed that P8 and P9 had worked, with pure products of the expected size seen, but no product was seen for P10.
- glgC mutagenesis: Transformed competent cells with ligation products L6 and L7; plated cells on Plates 22 and 23 (L6) and Plates 24 and 25 (L7).
- Ran gel 9 to check size of X1 (J33201) and X2 (pSB1A2+dxs) HindIII restriction digest. The digest looked fine.
