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Team:UNC Chapel Hill/19 June 2009
From 2009.igem.org
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| + | [[Team:UNC_Chapel_Hill/Notebook|Back]] | ||
*Met and talked about potential projects in detail | *Met and talked about potential projects in detail | ||
*Scott showed pictures of his results, transfecting the RFP part into bacteria: | *Scott showed pictures of his results, transfecting the RFP part into bacteria: | ||
[[Image:UNC-chapel-hill-190609.png]] | [[Image:UNC-chapel-hill-190609.png]] | ||
*Went over two projects: | *Went over two projects: | ||
| - | # Genetic Trigger Switch using Recombinases - The biological system | + | # Genetic Trigger Switch using Recombinases - The biological system will be in one state (say producing Red Fluorescent Proteins). A trigger will occur to induce the production of a recombinase, which will excise a sequence to put the system into another state (say producing Green Fluorescent Proteins). See attached for the presentation. |
| - | will be in one state (say producing Red Fluorescent Proteins). A | + | # Characterization system of iGem parts - Create a system to characterize various different iGem components using Fluorescent Proteins. For example, come up with a part with a blank spot for a promoter. This part would allow many different promoters to be compared. Could do similar tests on Ribosomal binding sites and Terminators. Would entail creating a detailed mathematical modeling system. Would also be immensely practical and useful for iGem. |
| - | trigger will occur to induce the production of a recombinase, which | + | |
| - | will excise a sequence to put the system into another state (say | + | |
| - | producing Green Fluorescent Proteins). See attached for the | + | |
| - | presentation. | + | |
| - | # Characterization system of iGem parts - Create a system to | + | |
| - | characterize various different iGem components using Fluorescent | + | |
| - | Proteins. For example, come up with a part with a blank spot for a | + | |
| - | promoter. This part would allow many different promoters to be | + | |
| - | compared. Could do similar tests on Ribosomal binding sites and | + | |
| - | Terminators. Would entail creating a detailed mathematical modeling | + | |
| - | system. Would also be immensely practical and useful for iGem. | + | |
*Will be voting on them by Monday. | *Will be voting on them by Monday. | ||
Latest revision as of 21:07, 22 June 2009
- Met and talked about potential projects in detail
- Scott showed pictures of his results, transfecting the RFP part into bacteria:
- Went over two projects:
- Genetic Trigger Switch using Recombinases - The biological system will be in one state (say producing Red Fluorescent Proteins). A trigger will occur to induce the production of a recombinase, which will excise a sequence to put the system into another state (say producing Green Fluorescent Proteins). See attached for the presentation.
- Characterization system of iGem parts - Create a system to characterize various different iGem components using Fluorescent Proteins. For example, come up with a part with a blank spot for a promoter. This part would allow many different promoters to be compared. Could do similar tests on Ribosomal binding sites and Terminators. Would entail creating a detailed mathematical modeling system. Would also be immensely practical and useful for iGem.
- Will be voting on them by Monday.
