Difference between revisions of "Summer 2013 SynBio Project (Davidson and MWSU)"
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High Priority = more people | High Priority = more people | ||
− | + | * eCDM8 working to make theophylline with biosensor and fitness modules (Tet^R) to report out. <br> | |
Which plasmid carries which device?<br> | Which plasmid carries which device?<br> | ||
− | + | * Determine the junction sequences and associated primers<br> | |
(use existing rules)<br> | (use existing rules)<br> | ||
build scaffold <br> | build scaffold <br> | ||
test JGG design<br> | test JGG design<br> | ||
− | + | * Stress module needs more work (see eCDM8 outputs)<br> | |
− | + | * test fitness module with adhE | |
compare with tetA<br> | compare with tetA<br> | ||
+ | fine tune tetA resistance<br> | ||
combine with tetA<br> | combine with tetA<br> | ||
− | + | * Copy number of plasmids <br> | |
+ | Can we alter Ori to produce a range of plasmid densities in ''E. coli''? <br> | ||
Lower Priority = one person | Lower Priority = one person |
Revision as of 14:01, 30 May 2013
Google Hangout 11 am Wednesday (10 Central)
Topics to Investigate
High Priority = more people
- eCDM8 working to make theophylline with biosensor and fitness modules (Tet^R) to report out.
Which plasmid carries which device?
- Determine the junction sequences and associated primers
(use existing rules)
build scaffold
test JGG design
- Stress module needs more work (see eCDM8 outputs)
- test fitness module with adhE
compare with tetA
fine tune tetA resistance
combine with tetA
- Copy number of plasmids
Can we alter Ori to produce a range of plasmid densities in E. coli?
Lower Priority = one person