Team:Calgary/1 September 2010
From 2010.igem.org
(New page: {{CalgaryNotebookTemplate| '''Wednesday September 1, 2010'''| Placeholder Text }}) |
|||
(3 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
{{CalgaryNotebookTemplate| | {{CalgaryNotebookTemplate| | ||
- | + | Wednesday September 1, 2010| | |
- | + | <u>Jeremy</u> | |
+ | |||
+ | Today I finished the protocols section for the wiki. I also made a figure for the poster. In the wetlab I ran the PCR on a gel and performed a gel purification. The purification failed so I have to do it again tomorrow. I also did overnights for MalE, MalE31, and nlpE. | ||
+ | |||
+ | |||
+ | <u>Himika</u> | ||
+ | |||
+ | Today I ran a colony PCR of the construction that I did last night. Unfortunately, the insert was not present in the amplified part. Therefore, I reconstructed the part which was MalE31 circuit with DegP+I13504 and I13507. I also worked more on the poster and presentation for aGEM. | ||
+ | |||
+ | |||
+ | <u>Chris</u> | ||
+ | |||
+ | Today, I took the plasmid preparations of CpxP done by Emily and did restriction digests of them as well as set up a colony PCR of them to be run on a gel. I also received confirmation from Autodesk and Nexen that they would be sponsoring us. With this, I contacted the people that could get the information to put this in motion. | ||
}} | }} |
Latest revision as of 03:37, 17 October 2010
Wednesday September 1, 2010
Jeremy
Today I finished the protocols section for the wiki. I also made a figure for the poster. In the wetlab I ran the PCR on a gel and performed a gel purification. The purification failed so I have to do it again tomorrow. I also did overnights for MalE, MalE31, and nlpE.
Himika
Today I ran a colony PCR of the construction that I did last night. Unfortunately, the insert was not present in the amplified part. Therefore, I reconstructed the part which was MalE31 circuit with DegP+I13504 and I13507. I also worked more on the poster and presentation for aGEM.
Chris
Today, I took the plasmid preparations of CpxP done by Emily and did restriction digests of them as well as set up a colony PCR of them to be run on a gel. I also received confirmation from Autodesk and Nexen that they would be sponsoring us. With this, I contacted the people that could get the information to put this in motion.