Team:Bielefeld-CeBiTec/Notebook/Journal/Isobutanol/Jul

From 2014.igem.org

(Difference between revisions)
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                       <li>PCR products were extracted out of the gel.</li>
                       <li>PCR products were extracted out of the gel.</li>
                       <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#DNAPurificationbyCentrifugation" target="_blank">Purfication</a> of the gel slices </li>
                       <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#DNAPurificationbyCentrifugation" target="_blank">Purfication</a> of the gel slices </li>
 +
                      <li>This worked well for <i>ilvC</i>, but not for <i>alsS</i>, <i>ilvD</i> and <i>kivD</i>.</li>
                   </ul>
                   </ul>
        </ul>
        </ul>

Revision as of 09:25, 2 October 2014


July

  • alsS, ilvC, ilvD, kivD and backbone of pSB1C3
    • We tried to redo the amplification of last week.
      • Optimization of PCR conditions for coding sequence amplification
        • Combinations of primers and templates as described before
        • Annealing temperature gradients from 50°C to 58°C were tried
        • Product amount was increased by lower annealing temperatures, but still not good enough for Gibson
  • alsS, ilvC, ilvD, kivD and backbone of pSB1C3
    • We tried to redo the amplification of last week.
      • Optimization of PCR conditions for coding sequence amplification
        • Combinations of primers and templates as described before
        • Annealing temperature gradients from 50°C to 58°C were tried
        • Product amount was increased by lower annealing temperatures
          • For the annealing temperature we identified 54°C as optimal.
          • For the elongation time 90 seconds worked better than 60 seconds.