Team:UT-Dallas/Notebook/8-04
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+ | <h1 class="firstHeading" align="center">Monday, August 4th, 2014 </h1> | ||
<center><p><a href="https://2014.igem.org/wiki/index.php?title=Team:UT-Dallas/Notebook/8-04&action=edit "style="color:#87A96B" >Click here to edit the page </a> </p></center> | <center><p><a href="https://2014.igem.org/wiki/index.php?title=Team:UT-Dallas/Notebook/8-04&action=edit "style="color:#87A96B" >Click here to edit the page </a> </p></center> | ||
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- | <p> | + | <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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<th><font size="3">Today's tasks:</font> | <th><font size="3">Today's tasks:</font> | ||
- | <p>Ligation. | + | <p>Transformed overnight Ligation.</p> |
<p>Digest more promoters.</p> | <p>Digest more promoters.</p> | ||
- | <p>Gel & gel purify reporter vectors | + | <p>Gel & gel purify reporter vectors.</p> |
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- | <br> | + | <br> Colonies!!!! |
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Latest revision as of 04:25, 17 October 2014
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Monday, August 4th, 2014
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:
Transformed overnight Ligation. Digest more promoters. Gel & gel purify reporter vectors. |
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