University of Arizona 2006
From 2006.igem.org
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==Meetings== | ==Meetings== | ||
| - | Next Meeting: Wed 7/ | + | Lab Work: All week: MWF in morning, afternoon |
| + | Next Meeting: Wed 7/17 in Shantz 440 | ||
==Resources== | ==Resources== | ||
Revision as of 04:07, 11 July 2006
University of Arizona 2006
Contents |
Team members
| Member | Contact | Role | |
|---|---|---|---|
| Joan Curry | curry@ag.arizona.edu | Faculty Advisor | |
| Mark Riley | riley@ag.arizona.edu | Faculty Advisor | |
| Patrick Hollinger | dogmod@email.arizona.edu | Biological Lab Work | |
| Josh Kittleson | jkittles@email.arizona.edu | ||
| Tim Spriggs | tims@u.arizona.edu | Project Manager / Documentation | |
| Tyler Brown | tylerb@email.arizona.edu | Documentation | |
| Dan Reavis | danman1@email.arizona.edu |
Meetings
Lab Work: All week: MWF in morning, afternoon Next Meeting: Wed 7/17 in Shantz 440
Resources
Local Resources
- [http://igem.engr.arizona.edu/phpBB2/ Team Forum]
Articles and References
Related Projects and Links
Projects
Our project ideas are still under development but for progress you may visit our Project Ideas.
We also maintain a forum for internal team communication. This is available at our [http://igem.engr.arizona.edu/phpBB2/ Team Forum].
The "Water Color" project (we don't have an official name yet) is the current project that we will be building. As of now, we will be focusing our attention on building this design. We want to start with a system that is not complex and that is straightforward to build. So that we can learn while we build. We want to add complexity later, after we have made what is already designed.
Project Details
The current name of our project is "Water Color." It is a system that selectively expresses one of three florescence proteins. Each of the three florescence proteins will be expressed in the presence of a unique inducer. Each florescent protein will be controlled by a unique repressed promoter.
The idea of our project is to have a media with these cells on it so that each cell will be individually activated to shown a certain "color" (in actuallity, express one florescent protein, which may or may not look unique). Thus the media is able to dispaly an image. A further idea, to be implemented later, is to have the ability to "erase" the image. This would be accomplished by repressing all three promoters.
All the requisite parts have been identified from the registry, and will be built together. (More detail on the specific part numbers and a diagram will be added later)
After the challenges of the first aspect of the project are overcome, more mechanical challenges still exist. For example: How to place the inducers?, or What scale should the image be?, or Are any optical techniques needed to fully visualize the image?
The first idea to place the inducers on the media is to use an injet printer. The printer could print solutions of inducers on a thin sheet which can be placed onto the media to put the inducers in contact with the cells. Issues that arrise are:
- The size of molecules and the aperature of the jet
- The fulid properties of the solution (e.g. viscosity) should match ink
- The sheet needs to effectively transfer the solutions to the media without mixing of regions
Photos
Team photo shown above, more to come.
