Team:KULeuven/Data
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<img src="http://homes.esat.kuleuven.be/~igemwiki/images/data/figure01.png"><br><br> | <img src="http://homes.esat.kuleuven.be/~igemwiki/images/data/figure01.png"><br><br> | ||
- | The first illustration is a global overview of our project in which you can see how the plasmids (and the parts) function in our system. The next illustration shows the plasmids | + | The first illustration is a global overview of our project in which you can see how the plasmids (and the parts) function in our system. The next illustration shows the plasmids in more detail, with the favorite new parts and the characterized pre-existing parts. <br> |
<img src="http://homes.esat.kuleuven.be/~igemwiki/images/data/figure02.png"><br><br> | <img src="http://homes.esat.kuleuven.be/~igemwiki/images/data/figure02.png"><br><br> |
Revision as of 16:03, 21 September 2011
Data page
How does E.D. Frosti work?
The first illustration is a global overview of our project in which you can see how the plasmids (and the parts) function in our system. The next illustration shows the plasmids in more detail, with the favorite new parts and the characterized pre-existing parts.
Plasmid 1 contains BBa_K584028 that enables E.D. Frosti to immediately respond to lactose and produce INP. BBa_K584027 is a precursor of BBa_K584028, with a constitutive promoter.
Plasmid 2 contains BBa_K584020 for AFP production. We were able to put AFP behind a constitutive promoter (BBa_K584026) but due to lack of time we could not finish the AFP stimulating system.
Plasmid 3 contains BBa_K584004. This is a GFP-construct to test the activity of the HybB promoter. Due to lack of time we could not test this biobrick. We wanted to engineer a biobrick in which the ribokey is controlled by the HybB promoter. BBa_K584027 was inserted in plasmid 1 to characterize INP.