Team:INSA Toulouse/contenu/lab practice/notebook/calendar/general inducer

From 2013.igem.org

(Difference between revisions)
Line 114: Line 114:
   <li><span class="spantitle2">Week 3 (24-30 June)</span></br>
   <li><span class="spantitle2">Week 3 (24-30 June)</span></br>
Amplification of new biobricks for cloning: <br>
Amplification of new biobricks for cloning: <br>
-
BBa_J23119: Strong promoter,
+
BBa_J23119: Strong promoter,<br>
-
BBa_P0440: rbs tetR term,
+
BBa_P0440: rbs tetR term,<br>
BBa_I13521: Ptet rbs RFP term.</li>
BBa_I13521: Ptet rbs RFP term.</li>
   </ul>
   </ul>

Revision as of 08:11, 19 September 2013

logo


Calendar

General Inducer Characterization

  • June 2013
    • Week 3 (24-30 June)
      Amplification of new biobricks for cloning:
      BBa_J23119: Strong promoter,
      BBa_P0440: rbs tetR term,
      BBa_I13521: Ptet rbs RFP term.
  • July 2013
    • Week 4 (1-7 July)
      Assembly of a strong promoter with tetR. tetR protein in necessary to inhibits the Ptet promoter.
    • Week 5 (8-14 July)
      Assembly of Strong promoter-tetR with Ptet-RFP. The RFP should be inhibited by tetR and expressed in presence of AHL.

      The construction is then sent for sequencing.

    • Week 6 (15-21 July)
      The sequencing shows that the construction include a mutated promoter instead of J23119. So we assembled tetR with Ptet-RFP.
    • Week 7 (22-28 July)
      We assembled a Strong promoter with tetR-Ptet-RFP to finalize the construction.

  • August 2013
    • Week 8 (29-4 August)
      The tries didn’t work, so we did it again one more week the assembly of Strong Promoter with tetR-Ptet-RFP.

    • Week 9 (5-11 August)
      Because none of last clonages worked, we tried with several promoters in order to increase our chances of success.
    • Week 10 (12-18 August)
      None of the passed assemblies worked, so we tried with a weak promoter.
    • Week 11 (19-25 August)


Back to Wet Lab