Team:UT-Dallas/Notebook/8-04

From 2014.igem.org

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   <p> Short coloquial description of what we did today and why.  </p>
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   <p> Today we did a gel purification of our overnight digested promoter, inoculated any color colonies from chromoproteins,transformed ligation's for reporter vectors, and prepared gRNA vectors for sequencing  </p>
   <p> Tentative plan for tomorrow </P>
   <p> Tentative plan for tomorrow </P>
    
    
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<p>Ligation. (over-night)</p>
<p>Ligation. (over-night)</p>
<p>Digest more promoters.</p>
<p>Digest more promoters.</p>
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<p>Gel & gel purify reporter vectors for stuffs that Sam picked.</p>
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<p>Gel & gel purify reporter vectors.</p>
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       <br> Colonies!!!!
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Revision as of 04:20, 17 October 2014

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

Monday, August 4th, 2014

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Today we did a gel purification of our overnight digested promoter, inoculated any color colonies from chromoproteins,transformed ligation's for reporter vectors, and prepared gRNA vectors for sequencing

Tentative plan for tomorrow

Today's tasks:

Ligation. (over-night)

Digest more promoters.

Gel & gel purify reporter vectors.
  • List item one
  • List item two
  • List item three
  • List item four
      <--------If you need subcategories--------->
    • Subcat 1
    • Subcat 2
    • Subcat 3
    • Subcat 4
  • List item five


Colonies!!!!

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