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

 
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<p> Document the dates you worked on your project.</p>
 
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</div>
 
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<div class="column half_size">
 
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<h5>What should this page have?</h5>
 
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<ul>
 
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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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<li>Pictures of your progress. </li>
 
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<li>Mention who participated in what task.</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>Inspiration</h5>
 
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<p>You can see what others teams have done to organize their notes:</p>
 
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<ul>
 
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<li><a href="https://2014.igem.org/Team:ATOMS-Turkiye/Notebook">2014 ATOMS-Turkiye</a></li>
 
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<li><a href="https://2014.igem.org/Team:Tec-Monterrey/ITESM14_project.html#tab_notebook">2014 Tec Monterrey</a></li>
 
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<li><a href="https://2014.igem.org/Team:Kyoto/Notebook/Magnetosome_Formation#title">2014 Kyoto</a></li>
 
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<li><a href="https://2014.igem.org/Team:Cornell/notebook">2014 Cornell</a></li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
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<hr>
 
 
<div align="center">
 
<div align="center">
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<h2> Week 1 (6/27 - 7/2) </h2>
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<h1> Lab Notebook </h1>
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<h4> 6/27 </h4>
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</div>
 
</div>
 
</div>
 
</div>
  
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<div class="column half_size">
 
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<h5> Cancer Group </h5>
 
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<ul>
 
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<li> PCR of 3xHA-TDGF1 construct. 12 cycles </li>
 
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<li> Gel of PCR Product → PCR was a failure. Band was 300bp. Should have been 750bp</li>
 
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<li> Second PCR of 3xHA-TDGF1 construct. 25 cycles instead of 12 → left overnight </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> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
  
 
<div class="column full_size">
 
<div class="column full_size">
 
<div align="center">
 
<div align="center">
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<h5> Interlab Study </h5>
 
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<ul>
 
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<li> Measured LUDOX and water for plate reader </li>
 
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<li> Transformation of positive and negative controls, test devices 1-3 </li>
 
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</ul>
 
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</div>
 
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</div>
 
  
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<div class="column full_size">
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W1">Week 1: 6/28 - 7/1 </a> </h1>
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<div align="center">
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<h4> 6/28</h4>
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</div>
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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>
 
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<li> Ran gel on PCR of yesterday's construct → Gel worked </li>
 
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<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> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h5> Interab Study </h5>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W2">Week 2: 7/4 - 7/8 </a> </h1>
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<ul>
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<li> Heat and "SB" streaking seems not to have worked</li>
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<li> No visible red colonies on plate </li>
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</ul>
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</div>
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</div>
 
</div>
  
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h4> 6/29 </h4>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W3">Week 3: 7/11 - 7/17 </a> </h1>
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</div>
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</div>
 
</div>
  
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<div class="column half_size">
 
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<h5> Cancer Group </h5>
 
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<ul>
 
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<li> PCR Not working well → keep trying new methods with different annealing temperatures </li>
 
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<li> Tried 65 and 67 degrees C</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> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h5> Interlab Study </h5>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W4">Week 4: 7/18 - 7/24</a></h1>
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<ul>
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<li> FITC started </li>
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<li> Cutting re-inoculated </li>
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<li> Ordered new LUDOX </li>
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</div>
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</div>
 
</div>
  
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h5> Other </h5>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W5">Week 5: 7/25 - 7/31</a> </h1>
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<ul>
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<li> College of Arts and Sciences Pre College Summer Institute students stopped by lab </li>
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<li> Spoke to them about information on synthetic biology and iGEM </li>  
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</div>
 
</div>
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</div>
 
  
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h4> 6/30 </h4>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W6">Week 6: 8/1 - 8/7</a></h1>
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</div>
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</div>
 
</div>
  
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<div class="column half_size">
 
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<h5> Cancer Group </h5>
 
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<ul>
 
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<li> PCR worked → Test 5 → changed annealing temperature to 66 degrees C + increased the denaturing time </li>
 
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<li> Nanodropped DNA</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> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h4> 7/1 </h4>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W7">Week 7: 8/8 - 8/14</a></h1>
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</div>
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</div>
 
</div>
  
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<div class="column half_size">
 
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<h5> Cancer Group </h5>
 
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<ul>
 
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<li> Digestion of TDGF-1 construct and YFP352GAP vector with two restriction enzymes </li>
 
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<li> Will ligate later </li>
 
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</ul>
 
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<table border=1>
 
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<tr>
 
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<td></td>
 
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<td>TDGF-1 Construct (Phire PCR 128.2 ng/mL)</td>
 
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<td>YEP352GAP Vector (343.2 ng/mL)</td>
 
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</tr>
 
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<tr>
 
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<td>Total Reaction Volume</td>
 
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<td>50 uL</td>
 
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<td>50 uL</td>
 
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</tr>
 
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<tr>
 
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<td>Nuclease Free Water</td>
 
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<td>27.4 uL</td>
 
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<td>37.2 uL</td>
 
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</tr>
 
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<tr>
 
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<td>10x Cutsmart Buffer</td>
 
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<td>5 uL</td>
 
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<td>5uL</td>
 
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</tr>
 
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<tr>
 
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<td>xho1</td>
 
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<td>1 uL</td>
 
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<td>1 uL</td>
 
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</tr>
 
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<tr>
 
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<td>Pvu II</td>
 
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<td>1 uL</td>
 
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<Td>1 uL</td>
 
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</tr>
 
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<tr>
 
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<td>DNA</td>
 
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<td>15.6 uL</td>
 
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<td>5.8 uL</td>
 
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</tr>
 
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</table>
 
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</div>
 
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<div class="column half_size">
 
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<h5> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h4> 7/2 </h4>
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<h1> <a id="stuff"href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W8">Week 8: 8/15 - 8/21</a> </h1>
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</div>
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</div>
 
</div>
  
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<div class="column half_size">
 
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<h5> Cancer Group </h5>
 
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<ul>
 
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<li> Running yesterday's digestion on gel </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h2> Week 2 (7/5-7/8) </h2>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W9">Week 9: 8/22 - 8/28</a></h1>
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<h4> 7/5 </h4>
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</dv>
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</div>
 
</div>
  
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<div class="column half_size">
 
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<h5> Cancer Group </h5>
 
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<ul>
 
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<li> Ran the PCR'ed construct on a gel with Phire Polymerase → It didn't work
 
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</ul>
 
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</div>
 
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<div class="column half_size">
 
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<h5> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h4> 7/6 </h4>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W10"> Week 10: 8/29 - 9/4 </a> </h1>
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</div>
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</div>
 
</div>
  
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<div class="column half_size">
 
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<h5> Cancer group </h5>
 
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<ul>
 
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<li> Ran the construct with PCR on gel → it worked </li>
 
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<li> Tasnia stabbed our gel </li>
 
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<li> Interlab study continues </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> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h4> 7/7 </h4>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W11"> Week 11: 9/5 - 9/11 </a> </h1>  
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</div>
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</div>  
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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>
 
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<li> Nanodrops were pretty low (84-120 ng/nl) </li>
 
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<li> 11:46am PCR'ed the highest nanodrop result in tube #1 → PCR successful </li>
 
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<li> 2:33pm → attempt to digest with remaining non-PCR product → removed from incubator at 5:00pm </li>
 
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<li> Made a gel → ran PCR </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> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
 
<div align="center">
 
<div align="center">
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<h2> Week 3 (7/11-7//15) </h2>
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<h1> <a id="stuff" href="https://2016.igem.org/Team:Stony_Brook/Notebook/Cancer-W14"> Week 12: 9/26 - 10/2 </a> </h1>
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<h4> 7/11 </h4>
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</div>
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</div>
 
</div>
  
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<div class="column half_size">
 
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<h5> Cancer group </h5>
 
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<ul>
 
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<li> Ran PCR on the construct (5x) → gel did not work </li>
 
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<li> PCR'ed 84.2 ng/ml construct </li>
 
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<li> 5 replicates made using Phire </li>
 
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<li><h1> Insert Table </h1></li>
 
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<li> Restreaking of YEP352GAP transformed cells for miniprep</li>
 
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<li> Restreaking placed in incubator at 12am</li>
 
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</div>
 
  
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<div class="column half_size">
 
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<h5> Vaccine Group </h5>
 
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<ul>
 
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<li> Stuff & Things </li>
 
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</ul>
 
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</div>
 
  
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<div class="column full_size">
 
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<div align="center">
 
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<h4> 7/12 </h4>
 
 
</div>
 
</div>
 
</div>
 
</div>
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<div class="column half_size">
 
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<h5> Cancer group </h5>
 
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<ul>
 
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<li> Made gel for electrophoresis of PCR construct → it didn't work </li>
 
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<li><h1> Insert table here</h1></li>
 
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<li> LB liquid culture (3ml with 3ul of ampicillin) </li>
 
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<li> Loaded 10ul Ladder DNA. </li>
 
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<li> Loaded 1ul dye + 5ul PCR product </li>
 
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<li> Ran gel at 115V </li>
 
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<li> Checked gel ladder → faint, no band for the PCR product </li>
 
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<li> Made new gel, loaded with the same amount of reagents as before → ran at 90V → No ladder band </li>
 
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<li> Ran it again at 115V → visible ladder, no PCR band </li>
 
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<li> Preparing a gel to run ladder and construct that previously showed a strong band → used this to diagnose a problem with gel setup. Ran TDGF1 152.9 Phire Child. Lane 1 is ladder, Lane 2 is that construct (10ul) with 2ul of dye </li>
 
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<li> Setup new PCR using the 6/30/16 PCR construct </li>
 
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</ul>
 
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<ol>
 
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<li> 98°C → 30sec </li>
 
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<li> 98°C → 20sec </li>
 
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<li> 66°C → 5sec </li>
 
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<li> 72°C → 30sec </li>
 
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<li> 72°C → 1min </li>
 
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<li> 4°C → hold </li>
 
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</ol>
 
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</div>
 
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<div class="column half_size">
 
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<h5> Vaccine Group </h5>
 
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<ul>
 
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<li> Stuff & Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
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<div align="center">
 
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<h4> 7/13 </h4>
 
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</div>
 
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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>
 
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<li> Ran 5ul of PCR with ladder, cancer construct and vaccine construct → to diagnose problem with gel </li>
 
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<li> Miniprep of Dean vector (3ml LB culture) </li>
 
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<li> Purification of PCR product → nanodropped 16.4ug/ul </li>
 
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<li> Nanodrop of: </li>
 
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</ul>
 
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<ol>
 
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<li> Yellow 7/13 construct NEB purified → 16.4ng/ml</li>
 
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<li> Blue gel purification → 48.7ng/ul</li>
 
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<li> Pink PCR purification 7/13 → 102.2ng/ul</li>
 
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<li>7/13 -RK Vector 1 → 48.2ng/ul</li>
 
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<li> 7/13 -RK Vector 2 → 96.3ng/ul</li>
 
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</ol>
 
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</div>
 
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<div class="column half_size">
 
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<h5> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
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<div align="center">
 
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<h4> 7/14</h4>
 
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</div>
 
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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>
 
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<li>Things</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> Vaccine Group </h5>
 
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<ul>
 
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<li> Things </li>
 
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</ul>
 
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</div>
 
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<div class="column full_size">
 
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<div align="center">
 
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<h5> Biobrick ideas </h5>
 
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<ol>
 
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<li> Smelly yeast → optimized from e. coli </li>
 
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<li> Twist on smelly e. coli on e. coli → regulated with quorum sensing</li>
 
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<li> OmpA/EnvZ recognize osmolarity</li>
 
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<li>Genetic Circuit</li>
 
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<li> Shine yellow light → Banana smell. Shine green light → wintergreen </li>
 
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<li> TetR operator system genetic circuit </li>
 
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<li> Have cell die at certain wavelength → killswitch </li>
 
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</ol>
 
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</div>
 
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</div>
 
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<div class="column full_size">
 
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<hr>
 
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Latest revision as of 07:53, 19 October 2016

Lab Notebook