IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Notes: Difference between revisions

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<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Modelling|Modelling]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Modelling|Modelling]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Implementation|Fabrication]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Implementation|Fabrication]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/TestingValidation|Testing/Validation]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/TestingValidation|Testing]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Data Analysis|Data Analysis]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Validation|Validation]]</li>
<li id="current">[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Notes|Notes]]</li>
<li id="current">[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Notes|Notes]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/References|References]]</li>
<li>[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/References|References]]</li>

Revision as of 05:28, 11 September 2007

Infector Detector: Notes



Making Biofilm

  • Freshly-grown growth-phase E. coli ZK1056 culture is added to sterile medium to a concentration of 5 × 107 cells/mL.
  • Round 15 mm sterile glass coverslips are placed upright in the wells of a 24-well plate with sterile plastic stands
  • Add 1 mL of E. coli solution to each well.
  • The 24-well plate is immediately covered and transferred to a 30 °C incubator.