Difference between revisions of "Missouri Western/Davidson iGEM2009"
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#[[What is the sequence of bacterial reverse transcriptase and can we clone that gene?]] | #[[What is the sequence of bacterial reverse transcriptase and can we clone that gene?]] | ||
#[[Can we redesign the normal msDNA pathway to produce new segments of DNA of our choosing?]] | #[[Can we redesign the normal msDNA pathway to produce new segments of DNA of our choosing?]] | ||
+ | #[[Can we use suppressor tRNAs to encode logical operators?]] | ||
+ | #[[What role can physical modeling of protein structure play in our project?]] | ||
Revision as of 16:20, 3 April 2009
This space will be used starting April, 2009 for brainstorming and a shared whiteboard space.
Davidson Lab Protocols
MWSU Lab Protocols
BioMath Connections Page
GCAT-along Freezer Stocks
We need to learn more about these topics:
- What is msDNA?
- How is msDNA normally produced?
- How is msDNA stored in E. coli?
- How many copies are carried per cell?
- What is the sequence of bacterial reverse transcriptase and can we clone that gene?
- Can we redesign the normal msDNA pathway to produce new segments of DNA of our choosing?
- Can we use suppressor tRNAs to encode logical operators?
- What role can physical modeling of protein structure play in our project?
- What interesting challenges or problems does origami offer?
- Can we produce a series of increasingly difficult goals that might be possible to produce in the lab?
- What has been done before and how can we improve upon that?
- We can perform some pilot experiments using synthesized DNA and later switch to msDNA (maybe).