Difference between revisions of "Team:ETH Zurich/Basic Part"
| Line 50: | Line 50: | ||
<tr> | <tr> | ||
<td>LldR</td> | <td>LldR</td> | ||
| − | <td> | + | <td>lldR </td> |
| + | <td><a href="http://parts.igem.org/Part:BBa_K1847001">BBa_K1847001</a></td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td>LldP-LldR</td> | ||
| + | <td>lldP-lldR </td> | ||
<td><a href="http://parts.igem.org/Part:BBa_K1847001">BBa_K1847001</a></td> | <td><a href="http://parts.igem.org/Part:BBa_K1847001">BBa_K1847001</a></td> | ||
</tr> | </tr> | ||
Revision as of 17:23, 16 September 2015
- Project
- Modeling
- Lab
- Human
Practices - Parts
- About Us
Basic Parts
In this section we present our basic parts. We expressed human Annexin V in Escherichia coli and then made a phusion protein with Annexin V and the Ice Nucleation Protein (INP). The former was created to allow our bacteria to serve as detectors of apoptosis by specifically binding phosphatidylserine.
Our other part is LldR, a protein required to regulate the lldR promoter. The expression of LldR was necessary to characterize the natural and our designed lldR promoters.
Part |
Content |
Registry number |
| Annexin V | Promoter J23114-RBS B0034- Annexin V optimized for Escherichia coli | BBa_K1847000 |
| INP-Annexin V | Promoter J23114-RBS B0034- INP-Annexin V fusion protein | BBa_K1847015 |
| LldR | lldR | BBa_K1847001 |
| LldP-LldR | lldP-lldR | BBa_K1847001 |
We would like to thank our sponsors
