Difference between revisions of "Team:DTU-Denmark/Notebook"

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            <li class="active"><a href="#week27">Week27</a></li>
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            <li><a href="#week28">Week28</a></li>
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            <li><a href="#week29">Week29</a></li>
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      <h3 id="week1">Week 1 (June 2 - June 8)</h3>
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<h4 class="media heading">Wet Lab Overview</h4>
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Transformation efficiency and protocols were tested - heat shock did not work well, and we came to the conclusion to stick with electroporation.
  
 
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The first day of Wet Lab training began on the 7th! We started working on amplification of metallothionein genes - so far nixA and GST-PMT appear to be working.
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<h3>What should this page have?</h3>
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<li>Chronological notes of what your team is doing.</li>
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<li> Brief descriptions of daily important events.</li>
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<img class="media object pull-left" src="https://static.igem.org/mediawiki/2014/2/28/Cornell-nb-dry.png">
<li>Pictures of your progress. </li>
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<li>Mention who participated in what task.</li>
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<h4 class="media heading">Dry Lab Overview</h4>
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Today was the first Dry Lab meeting for the new project! We discussed the mechanics and optimization of general filtration systems. We also started looking for the best way to make hollow fiber reactors the focal point of our filtration system.
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<h3>Inspiration</h3>
 
<p>You can see what others teams have done to organize their notes:</p>
 
 
<ul>
 
<li><a href="https://2014.igem.org/Team:ATOMS-Turkiye/Notebook">2014 ATOMS-Turkiye</a></li>
 
<li><a href="https://2014.igem.org/Team:Tec-Monterrey/ITESM14_project.html#tab_notebook">2014 Tec Monterrey</a></li>
 
<li><a href="https://2014.igem.org/Team:Kyoto/Notebook/Magnetosome_Formation#title">2014 Kyoto</a></li>
 
<li><a href="https://2014.igem.org/Team:Cornell/notebook">2014 Cornell</a></li>
 
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Revision as of 13:15, 16 July 2018

Notebook

Document the dates you worked on your project. This should be a detailed account of the work done each day for your project.

Week 1 (June 2 - June 8)


  • Wet Lab Overview

    Transformation efficiency and protocols were tested - heat shock did not work well, and we came to the conclusion to stick with electroporation. The first day of Wet Lab training began on the 7th! We started working on amplification of metallothionein genes - so far nixA and GST-PMT appear to be working.

  • Dry Lab Overview

    Today was the first Dry Lab meeting for the new project! We discussed the mechanics and optimization of general filtration systems. We also started looking for the best way to make hollow fiber reactors the focal point of our filtration system.