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Team:ETH Zurich/lab/overview
From 2014.igem.org
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* Can we produce a millifluidic PDMS chip with a 3D-printed mold? | * Can we produce a millifluidic PDMS chip with a 3D-printed mold? | ||
* Do ''E. coli'' cells still grow and produce fluorescent proteins and signal molecules when encapsulated into alginate beads? | * Do ''E. coli'' cells still grow and produce fluorescent proteins and signal molecules when encapsulated into alginate beads? | ||
| - | * | + | * Can the signal diffuse through the channels of the millifluidic chip and activate the cells in the neighboring bead? |
| + | * Is there crosstalk between the different quorum sensing systems? | ||
| + | * Do riboregulators decrease the problem of leakiness? | ||
| + | * Are the integrase based logic gates working in our setup? | ||
Click on the different subunits to learn more about how we worked in the lab and what our [https://2014.igem.org/Team:ETH_Zurich/expresults results] were. | Click on the different subunits to learn more about how we worked in the lab and what our [https://2014.igem.org/Team:ETH_Zurich/expresults results] were. | ||
Revision as of 14:38, 15 October 2014
Lab overview
- Can we produce a millifluidic PDMS chip with a 3D-printed mold?
- Do E. coli cells still grow and produce fluorescent proteins and signal molecules when encapsulated into alginate beads?
- Can the signal diffuse through the channels of the millifluidic chip and activate the cells in the neighboring bead?
- Is there crosstalk between the different quorum sensing systems?
- Do riboregulators decrease the problem of leakiness?
- Are the integrase based logic gates working in our setup?
Click on the different subunits to learn more about how we worked in the lab and what our results were.
