Difference between revisions of "Missouri Western/Davidson iGEM2009"
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#What is msDNA? | #What is msDNA? | ||
#How is msDNA normally produced? | #How is msDNA normally produced? | ||
− | #How is msDNA stored in E. coli? How many copies are carried per cell? | + | #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? | #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? |
Revision as of 19:32, 2 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?
- 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).
- What constructs are we testing?
- What school districts do we have access to?
- Where is the Synthetic Biology page we want high school teachers to use after the survey?
- Do you need any more input from the veterans before the survey is ready?