Team:UT-Dallas/Notebook/8-11

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<h1 class="firstHeading" align="center">Sunday, August 10, 2014</h1>
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<a href="https://2014.igem.org/Team:UT-Dallas"style="color:#ffffff; text-decoration: none; text-transform: uppercase; font-weight: bold;" >Home </a> </td>
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<a href="https://igem.org/Team.cgi?year=2014&team_name=UT-Dallas"style="color:#ffffff; text-decoration: none; text-transform: uppercase; font-weight: bold;"> Official Profile </a></td>
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<a href="https://2014.igem.org/Team:UT-Dallas/Attributions"style="color:#ffffff; text-decoration: none; text-transform: uppercase; font-weight: bold;"> Attributions </a></td>
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<a href="https://2014.igem.org/Team:UT-Dallas/Human-Practices"style="color:#ffffff; text-decoration: none; text-transform: uppercase; font-weight: bold;"> Human Practices</a></td>
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<h1 class="firstHeading" align="center">Monday, August 11, 2014</h1>
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<center><p><a href="https://2014.igem.org/wiki/index.php?title=Team:UT-Dallas/Notebook/8-11&action=edit "style="color:#87A96B" >Click here to edit the page </a> </p></center>
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  <p> Purified plasmid DNA from potential Reporter clones for later testing.  </p>
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   <p> Test purified plasmid DNA for correct insert. </P>
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   A short meeting (2 hours) to discuss our progress so far and further prospective of our project.</p>
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  We have a set of reporter vectors that we grew and harvested the DNA last week. Today, to qualitatively check that we got what we want, we are going to test digest our reporter vectors. After the check, we will send our second batch of sequencing order.</p>
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<p class="tab">Kristina brought lots of food: cookies, muffins, etc. We also have a dry ice party at the end of lab day!
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       <th><font size="3">Today's tasks:</font>
       <th><font size="3">Today's tasks:</font>
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<p>Miniprep</p>
 
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<p>Inoculated more clones</p>
 
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<LI> Miniprep potential transformants containing Reporter plasmids for ctxB, tcpJ, tcpP, and tcpS
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<LI> Miniprep tcpS clones
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         <LI> Clone inoculated from tcpS plate did not show expected yellow phenotype. 2 additional clones from the tcpS plate were inoculated in Chloramphenicol broth overnight to be purified and tested on Monday.  
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<LI> Test digest Reporter plasmids for ctxA, tcpJ, tcpP, and tcpS
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         <LI> Streak M13.
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<LI> Ligate + transform chromoproteins [P+RBS+chromo]
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<LI> Set up overnight ligation for tcpD, toxT.
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       <br> Preparing cells for plasmid purification.
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       <br> Megan Preparing cells for plasmid purification.
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  <br> Megan and tra playing with dry ice during down time
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Latest revision as of 04:04, 17 October 2014

Home Team Official Profile Project Parts Modeling Notebook Safety Attributions Human Practices

Monday, August 11, 2014

Click here to edit the page


A short meeting (2 hours) to discuss our progress so far and further prospective of our project.

We have a set of reporter vectors that we grew and harvested the DNA last week. Today, to qualitatively check that we got what we want, we are going to test digest our reporter vectors. After the check, we will send our second batch of sequencing order.

Kristina brought lots of food: cookies, muffins, etc. We also have a dry ice party at the end of lab day!

Today's tasks:

  • Miniprep tcpS clones
  • Test digest Reporter plasmids for ctxA, tcpJ, tcpP, and tcpS
  • Streak M13.
  • Ligate + transform chromoproteins [P+RBS+chromo]
  • Set up overnight ligation for tcpD, toxT.



Megan Preparing cells for plasmid purification.


Megan and tra playing with dry ice during down time