Line 37: | Line 37: | ||
<div align="center"> | <div align="center"> | ||
<h2> Week 1 (6/27 - 7/1) </h2> | <h2> Week 1 (6/27 - 7/1) </h2> | ||
− | <h4> 6/27 | + | <h4> 6/27 </h4> |
</div> | </div> | ||
</div> | </div> | ||
Line 60: | Line 60: | ||
<div class="column full_size"> | <div class="column full_size"> | ||
<div align="center"> | <div align="center"> | ||
− | <h4> 6/28 | + | <h4> 6/28</h4> |
</div> | </div> | ||
</div> | </div> | ||
Line 81: | Line 81: | ||
</ul> | </ul> | ||
</div> | </div> | ||
+ | |||
+ | <div class="column full_size"> | ||
+ | <div align="center"> | ||
+ | <h4> 6/29 </h4> | ||
+ | </div> | ||
+ | </div> | ||
+ | |||
+ | <div class="column half_size"> | ||
+ | <h5> Cancer Group </h5> | ||
+ | <ul> | ||
+ | <li> PCR Not working well → keep trying new methods with different annealing temperatures </li> | ||
+ | <li> Tried 65 and 67 degrees C</li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | |||
+ | <div class="column half_size"> | ||
+ | <h5> Interlab Study </h5> | ||
+ | <ul> | ||
+ | <li> FITC started </li> | ||
+ | <li> Cutting re-inoculated </li> | ||
+ | <li> Ordered new LUDOX </li> | ||
+ | |||
+ | <div class="column full_size"> | ||
+ | <div align="center"> | ||
+ | <h5> Other </h5> | ||
+ | <ul> | ||
+ | <li> College of Arts and Sciences Pre College Summer Institute students stopped by lab </li> | ||
+ | <li> Spoke to them about information on synthetic biology and iGEM </li> | ||
+ | </div> | ||
+ | </div> | ||
+ | |||
</html> | </html> |
Revision as of 19:57, 12 July 2016
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
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
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
6/29
Cancer Group
- PCR Not working well → keep trying new methods with different annealing temperatures
- Tried 65 and 67 degrees C
Interlab Study
- FITC started
- Cutting re-inoculated
- Ordered new LUDOX
- College of Arts and Sciences Pre College Summer Institute students stopped by lab
- Spoke to them about information on synthetic biology and iGEM