Difference between revisions of "Missouri Western/Davidson iGEM2009"
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We need to learn more about these topics: | We need to learn more about these topics: | ||
<center>'''Biology-based'''</center> | <center>'''Biology-based'''</center> | ||
| − | #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''?]] |
| − | #What is the sequence of bacterial reverse transcriptase and can we clone that gene? | + | #[[How many copies are carried per cell?]] |
| − | #Can we redesign the normal msDNA pathway to produce new segments of DNA of our choosing? | + | #[[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?]] | ||
| Line 24: | Line 25: | ||
<center>'''Behavior-based'''</center> | <center>'''Behavior-based'''</center> | ||
| − | #What constructs are we testing? | + | #[[What constructs are we testing?]] |
| − | #What school districts do we have access to? | + | #[[What school districts do we have access to?]] |
| − | #Where is the Synthetic Biology page we want high school teachers to use after the survey? | + | #[[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? | + | #[[Do you need any more input from the veterans before the survey is ready?]] |
Revision as of 19:40, 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).
