Team:Evry/Notebook/w8

From 2013.igem.org

(Difference between revisions)
Line 9: Line 9:
We started the week by doing the golden gates over again, meaning the GG 3 and GG 2 (2.1 with FurBS 1, 2.2 with FurBS2 and 2.3 with FurBS3). In fact, our previous control positive had some unwanted white spots (01/08/13), thus suggesting some contaminations during the transformation step. curretnmy waiting
We started the week by doing the golden gates over again, meaning the GG 3 and GG 2 (2.1 with FurBS 1, 2.2 with FurBS2 and 2.3 with FurBS3). In fact, our previous control positive had some unwanted white spots (01/08/13), thus suggesting some contaminations during the transformation step. curretnmy waiting
</p>
</p>
 +
 +
 +
<p>
 +
We performed 7 golden gates.
 +
With prepared a mix for the 6 tubes :
 +
  <ul>
 +
    <li> 8,89 µl of 1A3 plasmide
 +
    <li> 12,18 µL of terminator
 +
    <li> 9,8 µL of T4 Buffer
 +
    <li> 3,5 µL of BSA
 +
    <li> 3,5 µL of T4 ligase
 +
  </ul>
 +
</p>
 +
<p>
</br>
</br>

Revision as of 10:12, 6 August 2013

Iron coli project

Week 8: 5th August - 11th August

Plasmide 3:

We started the week by doing the golden gates over again, meaning the GG 3 and GG 2 (2.1 with FurBS 1, 2.2 with FurBS2 and 2.3 with FurBS3). In fact, our previous control positive had some unwanted white spots (01/08/13), thus suggesting some contaminations during the transformation step. curretnmy waiting

We performed 7 golden gates. With prepared a mix for the 6 tubes :

  • 8,89 µl of 1A3 plasmide
  • 12,18 µL of terminator
  • 9,8 µL of T4 Buffer
  • 3,5 µL of BSA
  • 3,5 µL of T4 ligase


Additionnally, we did the optimization of our PCR over with the temperature gradient for the annealing step. current waiting