17/09/13
From 2013.igem.org
(Difference between revisions)
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*For digestion of backbone, already digested backbone from 01/08/2013 was used, which was digested with EcoRI and PstI. | *For digestion of backbone, already digested backbone from 01/08/2013 was used, which was digested with EcoRI and PstI. | ||
- | == | + | ==Incubation of bacteria from the plates of previous day for mini prep== |
+ | *12 single colonies were picked from each plate and put into 15ml of broth | ||
+ | *36 tubes were left incubating overnight at 37C | ||
+ | |||
+ | ==Sending pGEM-T vector with Tod insert clones to sequencing by PNACL== | ||
+ | |||
+ | ==Digestion of new fusion PCR Tod genes== | ||
+ | *Digestion with EcorI-HF and PstI-HF using Cutsmart buffer | ||
+ | {|border=1 | ||
+ | |Sample||DNA||Buffer||Water||EcorI-HF||PstI-HF | ||
+ | |- | ||
+ | |Tod X||10.1ul||3ul||15.9||0.5||0.5 | ||
+ | |- | ||
+ | |Tod F||13.4ul||3ul||12.6||0.5||0.5 | ||
+ | |- | ||
+ | |Tob B||14.7ul||3ul||11.3||0.5||0.5 | ||
+ | |} |
Revision as of 10:16, 18 September 2013
Contents |
Results from previous day
- Background control plate had growth, which was not expected. This suggests that pSB1C3 backbone religated.
- It was also thought that the Tod genes used were not from the PCR fusion experiment.
- Same experiment done again, with a new set of Tod genes from a PCR fusion.
- For digestion of backbone, already digested backbone from 01/08/2013 was used, which was digested with EcoRI and PstI.
Incubation of bacteria from the plates of previous day for mini prep
- 12 single colonies were picked from each plate and put into 15ml of broth
- 36 tubes were left incubating overnight at 37C
Sending pGEM-T vector with Tod insert clones to sequencing by PNACL
Digestion of new fusion PCR Tod genes
- Digestion with EcorI-HF and PstI-HF using Cutsmart buffer
Sample | DNA | Buffer | Water | EcorI-HF | PstI-HF |
Tod X | 10.1ul | 3ul | 15.9 | 0.5 | 0.5 |
Tod F | 13.4ul | 3ul | 12.6 | 0.5 | 0.5 |
Tob B | 14.7ul | 3ul | 11.3 | 0.5 | 0.5 |