Line 85: | Line 85: | ||
</p> | </p> | ||
<ul> | <ul> | ||
− | <li> | + | <li>Primers arrived</li> |
</ul> | </ul> | ||
</div> | </div> | ||
Line 92: | Line 92: | ||
<div class = "description"> | <div class = "description"> | ||
<p> | <p> | ||
− | <b>SUMMARY of August | + | <b>SUMMARY of August 1st: </b> |
</p> | </p> | ||
<ul> | <ul> | ||
Line 99: | Line 99: | ||
</div> | </div> | ||
+ | <h3 class = "day"> DAY 5 </h3> | ||
+ | |||
+ | <div class = "description"> | ||
+ | <p> | ||
+ | <b>SUMMARY of August 2nd: </b> | ||
+ | </p> | ||
+ | <ul> | ||
+ | <li>Received oligos </li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | |||
+ | <h3 class = "day"> DAY 6 </h3> | ||
+ | |||
+ | <div class = "description"> | ||
+ | <p> | ||
+ | <b>SUMMARY of August 7th: </b> | ||
+ | </p> | ||
+ | <ul> | ||
+ | <li>Digestion of lentiviral CRISPR plasmid </li> | ||
+ | <li>Gel purification digested plasmid using QIAquick Gel Extraction Kit and eluted in buffer EB</li> | ||
+ | <li>There should be two bands on the gel, one at 2kb which should not be purified. Purify only the larger band</li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | <h3 class = "day"> DAY 7 </h3> | ||
+ | |||
+ | <div class = "description"> | ||
+ | <p> | ||
+ | <b>SUMMARY of August 9th: </b> | ||
+ | </p> | ||
+ | <ul> | ||
+ | <li>Anneal oligo pairs </li> | ||
+ | <li>Ligation and transformation<li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | |||
+ | <h3 class = "day"> DAY 8 </h3> | ||
+ | |||
+ | <div class = "description"> | ||
+ | <p> | ||
+ | <b>SUMMARY of August 10th: </b> | ||
+ | </p> | ||
+ | <ul> | ||
+ | <li>No colonies grew on carb antibiotic plates </li> | ||
+ | </ul> | ||
+ | </div> | ||
</div> | </div> | ||
Revision as of 04:22, 15 October 2017
Lab Notebook
DAY 1
SUMMARY of July 17th:
- DNA extraction from GBM39 cells
- Agarose gel electrophoresis to confirm DNA
DAY 2
SUMMARY of July 18th:
- qPCR primer design and order
DAY 3
SUMMARY of July 21:
- Primers arrived
DAY 4
SUMMARY of August 1st:
DAY 5
SUMMARY of August 2nd:
- Received oligos
DAY 6
SUMMARY of August 7th:
- Digestion of lentiviral CRISPR plasmid
- Gel purification digested plasmid using QIAquick Gel Extraction Kit and eluted in buffer EB
- There should be two bands on the gel, one at 2kb which should not be purified. Purify only the larger band
DAY 7
SUMMARY of August 9th:
- Anneal oligo pairs
- Ligation and transformation
DAY 8
SUMMARY of August 10th:
- No colonies grew on carb antibiotic plates