Difference between revisions of "Team:Pasteur Paris/Demonstrate"

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Revision as of 19:05, 16 October 2018

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NERVE GROWTH FACTOR AND NEURON CULTURE

We successfully cloned a part coding for secretion of NGF in pET43.1a and iGEM plasmid backbone pSB1C3, creating a new part Bba_K2616000 and confirmed the production of proNGF by Western Blot and mass spectrometry.

We grew neurons on our self-made microfluidic chips ans successfully observe axon growth in the presence of commercial NGF

KILL SWITCH

Achievements:

  • Successfully cloned a part coding for toxin/antitoxin (CcdB/CcdA) system in iGEM plasmid backbone, creating a new basic part Bba_K2616002
  • Successfully sequenced BBa_K2616002 in pSB1C3 and sent to iGEM registry
  • Successfully observe survival of our engineered bacteria at 25°C and 37°C and absence of growth at 18°C and 20°C, showing the efficiency of the kill switch

Next steps:

  • Find a system that kills bacteria when released in the environment rather than just stopping their growth

MEMBRANE BIOCOMPATIBILITY AND CONDUCTIVITY

DESIGN