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Edinburgh/25 July 2008
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| - | ==== Friday 25 July 08 | + | <html> |
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| + | |align="left" width="150pt"|{{#calendar: title=Edinburgh |year=2008 | month=06}} | ||
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| + | |align="left" width="150pt"|{{#calendar: title=Edinburgh |year=2008 | month=08}} | ||
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| + | :::: '''[[Edinburgh/24_July_2008|< Previous Entry]]''' | ||
| + | |||
| + | == Week 6 == | ||
| + | === Friday 25 July 08 === | ||
* Made maxiprep '''X4''' (pSB1A2-''crtB'' as M36; BBa_K118002) and '''X5''' (pSB1A2-''crtI'' as M42; BBa_K118003) (AH, XH) | * Made maxiprep '''X4''' (pSB1A2-''crtB'' as M36; BBa_K118002) and '''X5''' (pSB1A2-''crtI'' as M42; BBa_K118003) (AH, XH) | ||
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* PCR '''P36''' of M43 (''glgC''-mut1,2) to excise the gene from BABEL and rectify its orientation and '''P37''' of ''crtY'' from ''P. ananatis'' (Plate 17) cell suspension - repeat of P27. | * PCR '''P36''' of M43 (''glgC''-mut1,2) to excise the gene from BABEL and rectify its orientation and '''P37''' of ''crtY'' from ''P. ananatis'' (Plate 17) cell suspension - repeat of P27. | ||
** P36 and P37 run on '''Gel 25'''. P36 tentatively successful (larger than desirable smear in the region of interest), P37 failed. | ** P36 and P37 run on '''Gel 25'''. P36 tentatively successful (larger than desirable smear in the region of interest), P37 failed. | ||
| - | * Also did preparations to transfer ''crtE'' from BABEL2 vector to pSB1A2. This is necessary, because we are supposed to use Registry standard vectors for all BioBricks we make (in fact, we should even stop using pSB1A2and move to pSB1A3). So, digested the BABEL2+''crtE'' clone that Douglas Leslie made with EcoRI and PstI, and also Edinbrick1 - in both cases, 3μl in 20μl total volume. Ran both on a gel and excised the appropriate bands, eluted each to 10μl EB and set up a ligation using 4μl of each in 10μl total volume. Ligated at 16°C. (CF) | + | * Also did preparations to transfer ''crtE'' from BABEL2 vector to pSB1A2. This is necessary, because we are supposed to use Registry standard vectors for all BioBricks we make (in fact, we should even stop using pSB1A2and move to pSB1A3). So, digested the BABEL2+''crtE'' clone that Douglas Leslie made with EcoRI and PstI, and also Edinbrick1 - in both cases, 3μl in 20μl total volume. Ran both on a gel and excised the appropriate bands, eluted each to 10μl EB and set up a ligation using 4μl of each in 10μl total volume. Ligated at 16°C. (CF)<br /> |
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| + | :::: '''[[Edinburgh/26_July_2008|Next Entry >]]''' | ||
Revision as of 11:57, 26 August 2008
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Week 6
Friday 25 July 08
- Made maxiprep X4 (pSB1A2-crtB as M36; BBa_K118002) and X5 (pSB1A2-crtI as M42; BBa_K118003) (AH, XH)
- Ligation of P29 into Edinbrick1 to make L22 (pSB1A2+rbs+crtI). (Yan, OG)
- Ligation of P28 into Edinbrick1 to make L21 (pSB1A2+rbs+crtB). (Yan, OG)
- Ligation of P12 into Edinbrick1 to make L19 (pSB1A2+rbs+dxs). (Yan, OG)
- Ligation of P15 into Edinbrick1 to make L20 (pSB1A2+rbs+appY). (Yan, OG)
- Ligation of P31 into Edinbrick1 to make L23 (pSB1A2+pZntA). (Yan, OG)
- C. fimi Plate 48 appears to be contaminated (mix of opaque and clear colonies). The same culture was used for genomic DNA purification yesterday ~ this preparation is therefore inadequate for sequencing purpose but might be worth using for PCR. (AM)
- No growth of C. fimi on Plates 49 and 50, but C. fimi takes a relatively long time to form colonies so we should check again on Monday. (AM)
- PCR P36 of M43 (glgC-mut1,2) to excise the gene from BABEL and rectify its orientation and P37 of crtY from P. ananatis (Plate 17) cell suspension - repeat of P27.
- P36 and P37 run on Gel 25. P36 tentatively successful (larger than desirable smear in the region of interest), P37 failed.
- Also did preparations to transfer crtE from BABEL2 vector to pSB1A2. This is necessary, because we are supposed to use Registry standard vectors for all BioBricks we make (in fact, we should even stop using pSB1A2and move to pSB1A3). So, digested the BABEL2+crtE clone that Douglas Leslie made with EcoRI and PstI, and also Edinbrick1 - in both cases, 3μl in 20μl total volume. Ran both on a gel and excised the appropriate bands, eluted each to 10μl EB and set up a ligation using 4μl of each in 10μl total volume. Ligated at 16°C. (CF)
