Team:ETH Zurich/Biology/Journal
From 2011.igem.org
(Difference between revisions)
Line 15: | Line 15: | ||
== ''' Week 3: 4.7-10.7''' == | == ''' Week 3: 4.7-10.7''' == | ||
- | * Design of several Operons for AlcR | + | * Design of several Operons for AlcR and several PCR primer |
+ | * Making of competent DH5-α cells | ||
== '''Week 4: 11.7-17.7''' == | == '''Week 4: 11.7-17.7''' == | ||
- | *Cloning of the | + | * Cloning of the AlcR-testsystem |
- | + | ||
== '''Week 5: 18.7-24.7''' == | == '''Week 5: 18.7-24.7''' == | ||
* First test of the AlcR-system in 96-well plates | * First test of the AlcR-system in 96-well plates | ||
- | |||
== '''Week 6: 25.7-31.7''' == | == '''Week 6: 25.7-31.7''' == | ||
+ | * Transformation of the parts from the iGEM plates | ||
== '''Week 7: 1.8-7.8''' == | == '''Week 7: 1.8-7.8''' == | ||
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** P<sub>lac</sub> and GFP<sub>LVA</sub> | ** P<sub>lac</sub> and GFP<sub>LVA</sub> | ||
** P<sub>lux</sub> and mCherry | ** P<sub>lux</sub> and mCherry | ||
- | ** P<sub>tet</sub> and CI | + | ** P<sub>tet</sub> and CI -had to be redone because of point mutation in the primer (week 9) |
** P<sub>const</sub> and luxR | ** P<sub>const</sub> and luxR | ||
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== '''Week 8: 8.8-14.8''' == | == '''Week 8: 8.8-14.8''' == | ||
- | Synthesized LacI<sub>M1</sub> Gen arrived | + | * Synthesized LacI<sub>M1</sub> Gen arrived |
* Ligation and Transformation of | * Ligation and Transformation of | ||
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** P<sub>lux</sub>-mCherry and Terminator | ** P<sub>lux</sub>-mCherry and Terminator | ||
** P<sub>const</sub>-luxR and Terminator | ** P<sub>const</sub>-luxR and Terminator | ||
+ | ** P<sub>lac</sub>-GFP<sub>LVA</sub>-Terminator and P<sub>lux</sub>-mCherry-Terminator on one plasmid | ||
+ | ** P<sub>tet</sub> and LacI<sub>M1</sub> | ||
+ | ** P<sub>tet</sub>-LacI<sub>M1</sub> and Terminator | ||
- | * Exchange of same rare codons in AlcR by PCR | + | |
+ | * Improving of the testsystem | ||
+ | ** Exchange of same rare codons in AlcR by PCR | ||
+ | ** His-tagging of AlcR | ||
+ | ** GFP assam | ||
* Transformation of λ<sub>P</sub> | * Transformation of λ<sub>P</sub> | ||
+ | |||
+ | * Making of competent JM101 cells | ||
+ | ** Check for transformation efficiency | ||
== '''Week 9: 15.8-21.8''' == | == '''Week 9: 15.8-21.8''' == | ||
- | + | * Growth and repression test of AlcR-system with M9-medium | |
- | + | * Ligation and Transformation of | |
+ | ** λ<sub>P</sub> and lacI | ||
+ | ** λ<sub>P</sub> and luxI | ||
+ | ** P<sub>tet</sub> and CI | ||
+ | ** λ<sub>P</sub>-lacI and terminator | ||
+ | ** λ<sub>P</sub>-luxI and terminator | ||
== '''Week 10: 22.8-28.8''' == | == '''Week 10: 22.8-28.8''' == |
Revision as of 12:54, 22 August 2011
Week 1: 20.6-26.6
- First meeting
- Brainstorming
Week 2: 27.6-3.7
- Brainstorming
Week 3: 4.7-10.7
- Design of several Operons for AlcR and several PCR primer
- Making of competent DH5-α cells
Week 4: 11.7-17.7
- 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
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