Difference between revisions of "Team:Stony Brook/Notebook"

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<li> PCR of 3xHA-TDGF1 construct </li>
 
<li> PCR of 3xHA-TDGF1 construct </li>
 
<li> Gel of PCR Product → PCR was a failure </li>
 
<li> Gel of PCR Product → PCR was a failure </li>
−
<li> Second PCR of 3xHA-TDGF1 construct → left overnight. </li>
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<li> Second PCR of 3xHA-TDGF1 construct → left overnight </li>
 
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<li> Measured LUDOX and water for plate reader </li>
 
<li> Measured LUDOX and water for plate reader </li>
 
<li> Transformation of positive and negative controls, test devices 1-3 </li>
 
<li> Transformation of positive and negative controls, test devices 1-3 </li>
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</ul>
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<div class="column full_size">
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<div align="center">
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<h4> 6/28/16</h4>
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</div>
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<div class="column half_size">
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<h5> Cancer Group </h5>
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<ul>
 +
<li> Ran gel on PCR of yesterday's construct → Gel worked </li>
 +
<li> Gel purification of PCR Product → low concentration of DNA found during nanodrop</li>
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<li> PCR the construct using a revised method </li>
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<li> 2:54pm → ran the gel on the PCR product </li>
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</ul>
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</div>
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<div class="column half_size">
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<h5> Interab Study </h5>
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<ul>
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<li> Heat and "SB" streaking seems not to have worked</li>
 +
<li> No visible red colonies on plate </li>
 
</ul>
 
</ul>
 
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Revision as of 19:46, 12 July 2016

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Document the dates you worked on your project.

What should this page have?
  • Chronological notes of what your team is doing.
  • Brief descriptions of daily important events.
  • Pictures of your progress.
  • Mention who participated in what task.
Inspiration

You can see what others teams have done to organize their notes:

Week 1 (6/27 - 7/1)

6/27/16

Cancer Group
  • PCR of 3xHA-TDGF1 construct
  • Gel of PCR Product → PCR was a failure
  • Second PCR of 3xHA-TDGF1 construct → left overnight
Interlab Study
  • Measured LUDOX and water for plate reader
  • Transformation of positive and negative controls, test devices 1-3

6/28/16

Cancer Group
  • Ran gel on PCR of yesterday's construct → Gel worked
  • Gel purification of PCR Product → low concentration of DNA found during nanodrop
  • PCR the construct using a revised method
  • 2:54pm → ran the gel on the PCR product
Interab Study
  • Heat and "SB" streaking seems not to have worked
  • No visible red colonies on plate