Team:Cambridge/Lab book/Week 11
From 2012.igem.org
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Revision as of 15:21, 14 September 2012
Week: | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 |
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Contents |
Monday (03/09/12)
Tuesday (04/09/12)
Wednesday (05/09/12)
PCR of biobrick fragments and MGRS construct fragments.
- Fluoride and magnesium riboswitch genomic DNA amplified with PCR, along with vector fragments for turning the MGRS into a biobrick and for producing the magnesium riboswitch construct.
- PCR settings: Annealing temperature - 58 °C, Elongation step - 60 seconds.
- Genomic fragments worked well, but longer backbone fragments mostly failed.
- Extractions of DNA from these gels failed almost completely. Will try purifying directly from PCR products next time - results may not produce such a high purity of the precise DNA we want, but the increase in yield should outweigh this problem.
Gibson assembly of -8 MGRS construct
- Fragments gel extracted earlier assembled with Gibson assembly.
- Fragments used:
- 9kbp fragment from tube 13 used as backbone.
- Genomic fragments from tubes 6 + 7.
Transformation of E.coli with Gibson products
- Gibson products from earlier today used to transform e.coli.
- Resultant transformants plated out on 100 μg/ml ampicillin plates.
Thursday (06/09/12)
Friday (07/09/12)
Saturday (08/09/12)
Gel for 9kb fragments of lux and flu construct:
File:Long frags PM 08.09.12.tif
Sunday (09/09/12)
Verification gel: