Team:Calgary/1 August 2010
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Emily Hicks (Talk | contribs) |
Emily Hicks (Talk | contribs) |
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<u>Emily</u> | <u>Emily</u> | ||
- | Heck yes we do! This evening I made overnight cultures of my hypotically biobricked malE and malE31 in TOPO BLUNT Vector. I also set up an overnight digest of . | + | Heck yes we do! This evening I made overnight cultures of my hypotically biobricked malE and malE31 in TOPO BLUNT Vector. I also set up an overnight digest of a construction of I0500-I13504 and I0500-I13507. I want to construct these circuits as a control for our Arabinose Induction tests. |
<u>Chris</u> | <u>Chris</u> |
Revision as of 13:50, 11 August 2010
Sunday August 1, 2010
Who wants to work on weekends? We do!!
Emily
Heck yes we do! This evening I made overnight cultures of my hypotically biobricked malE and malE31 in TOPO BLUNT Vector. I also set up an overnight digest of a construction of I0500-I13504 and I0500-I13507. I want to construct these circuits as a control for our Arabinose Induction tests.
Chris
Today, I went through PCR purifications of 100 µL of each of the CpxP Promoter PCR Products using a Qiagen kit with the same modified procedure as yesterday. This second purification was done to gain more purified product. Most of the first purification was used up in doing a restriction digest and attempting to construct the CpxP promoter into Ampicillin-kanamycin and ampicillin-chloramphenicol plasmids. I also did this construction today, cutting with the restriction enzymes XbaI and PstI.
Dev
Today I performed a plasmid switch of the CpxR promoter from an ampicillin resistant plasmid to an ampicillin-kanamycin resistant plasmid. Transformed the AK CpxR into competent cells and plated.
No notebook page exists for this date. Sorry!