Team:ETH Zurich/Biology/Journal
From 2011.igem.org
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- | |style="font-size:2em; | + | |style="font-size:2em; height: 30px" class="biology"|Lab Journal |
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- | {|class="biologyTitle" border="0" cellspacing="0" cellpadding="3" align="right" style="border-radius:10px; text-align:center; white-space:nowrap; color: black;" | + | {|class="biologyTitle linkMapJournal" border="0" cellspacing="0" cellpadding="3" align="right" style="border-radius:10px; text-align:center; white-space:nowrap; color: black;" |
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- | |style="color:white; width: 3em | + | |style="color:white; width: 3em; border-left: none;"|Week |
- | + | |[[#Week 1: 20.6-26.6|1]] | |
- | + | |[[#Week 2: 27.6-3.7|2]] | |
- | + | |[[#Week 3: 4.7-10.7|3]] | |
- | + | |[[#Week 4: 11.7-17.7|4]] | |
- | + | |[[#Week 5: 18.7-24.7|5]] | |
- | + | |[[#Week 6: 25.7-31.7|6]] | |
- | + | |[[#Week 7: 1.8-7.8|7]] | |
- | + | |[[#Week 8: 8.8-14.8|8]] | |
- | + | |[[#Week 9: 15.8-21.8|9]] | |
- | + | |[[#Week 10: 22.8-28.8|10]] | |
- | + | |[[#Week 11: 29.8-4.9|11]] | |
- | + | |[[#Week 12: 5.9.-11.9|12]] | |
- | + | |[[#Week 13: 12.9.-18.9|13]] | |
- | + | |[[#Week 14: 19.9.-25.9|14]] | |
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Revision as of 16:08, 10 September 2011
Lab Journal |
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Here you can follow the progress of our project as it is coming together. |
Week 1: 20.6-26.6
- First meeting
- Brainstorming
Week 2: 27.6-3.7
- Brainstorming
Week 3: 4.7-10.7
- Working on the design of the system
- Design of several Operons for AlcR and several PCR primer
Week 4: 11.7-17.7
- Ordering of the LacIM1 and codonoptimized AlcR gene
- Making of competent DH5-α cells
- Cloning of the AlcR-testsystem
Week 5: 18.7-24.7
- First test of the AlcR-system in 96-well plates
Week 6: 25.7-31.7
- Transformation of the parts from the iGEM plates
Week 7: 1.8-7.8
- Growth test of DH5-α with AlcR-system in flasks
- Ligation and Transformation of
- λP and luxI
- λP and lacI
- Plac and GFPLVA
- Plux and mCherry
- Ptet and CI -had to be redone because of point mutation in the primer (week 9)
- Pconst and luxR
- First meeting with Dr. Oliver Frey (Bio engineering laboratory, Prof. Andreas Hierlemann, D-BSSE ETHZ) to exchange ideas about microfluidic design
Week 8: 8.8-14.8
- Synthesized LacIM1 Gen arrived
- Ligation and Transformation of
- Plac-GFPLVA and Terminator
- Plux-mCherry and Terminator
- Pconst-luxR and Terminator
- Plac-GFPLVA-Terminator and Plux-mCherry-Terminator on one plasmid
- Ptet and LacIM1
- Ptet-LacIM1 and Terminator
- Improving of the testsystem
- Exchange of same rare codons in AlcR by PCR
- His-tagging of AlcR
- GFP assam
- Transformation of λP
- Making of competent JM101 cells
- Check for transformation efficiency
Week 9: 15.8-21.8
- Growth and repression test of AlcR-system with M9-medium
- Ligation and Transformation of
- λP and lacI
- λP and luxI
- Ptet and CI
- λP-lacI and terminator
- λP-luxI and terminator
Week 10: 22.8-28.8
- Transformation and Ligation
- Ptet-CI and Terminator
- Preparation of chemically competent DH5-α and JM101 cells
Week 11: 29.8-4.9
- Transformation and Ligation
- Ptet-CI and Terminator
- Diffusion test through tube system filled with agarose and cells
- Test of the improved AlcR system
Week 12: 5.9.-11.9
- Design of a system to characterize our new biobrick LacIM1
- Transformation and Ligation
- PTet and LacI
- PLac and GFP assam
- Transformation and Ligation
- Design of an additional construct to test the band pass filter
- Transformation and Ligation
- Pconst and TetRLVA
- Transformation and Ligation
- Growth-test of E.coli in M9 with reduced Ampicillin concentration
- AlcR test with reduced Ampicillin concentration
- Testdigest of λP-luxI-Terminator
- Alternative Sensor system: Xylene system
- Transformation and Ligation
- Pconst and XylR
- PXyl and CI
- PXyl and LacI M1
- Transformation and Ligation