Difference between revisions of "Summer 2013 SynBio Project (Davidson and MWSU)"
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'''Topics to Investigate''' | '''Topics to Investigate''' | ||
| − | High Priority = more people | + | <u>High Priority = more people</u> |
* eCDM8 working to make theophylline with biosensor and fitness modules (Tet^R) to report out. <br> | * eCDM8 working to make theophylline with biosensor and fitness modules (Tet^R) to report out. <br> | ||
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Can we alter Ori to produce a range of plasmid densities in ''E. coli''? <br> | Can we alter Ori to produce a range of plasmid densities in ''E. coli''? <br> | ||
| − | Lower Priority = one person | + | <u>Lower Priority = one person</u> |
<center>Mathematics</center> | <center>Mathematics</center> | ||
Revision as of 14:02, 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
