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Team:BYU Provo/Notebook/SmallPhage/Springexp/Period2/Dailylog
From 2013.igem.org
(Created page with "{{TeamBYUProvo}} <br> {| width="100%" | colspan="3" | <font color="#333399" size="5" font face="Calibri"> '''Small Phage Spring Notebook: May 13 - May 26 Daily Log'''</font> <...") |
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Revision as of 20:51, 27 May 2013
| Small Phage Spring Notebook: May 13 - May 26 Daily Log
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5/13/13 - Purified phage stock in 5.9 T7+ Liquid Culture Phage Concentration Test #2 - Performed 5.13 Determining E coli Concentration with Spectrophotometer - Started the registry for phage stock
5/14/13 - Started two 5mL BL21 overnight at 6:00pm
5/15/13 - Completed 5.9 T7+ Liquid Culture Phage Concentration Test #2 by doing the spot test - Performed 5.15 Titer Test on 5.3 T7 new Phage Stock to determine phage concentration and estimate dilution for applying mutagen - Sorted LB plates made on May 8 and threw away the ones with obvious contamination
5/16/13 - Took plates from 5.15 out of incubation at around 4:00pm
5/17/13 - Determined that all LB plates from 5.8 had contamination - Poured new LB plates - Made x8 top agar
5/18/13 - Stacked up the LB plates made yesterday. No obvious sign of contamination seen. - Threw away the 5.8 LB plates (the ones with contamination).
5/19/13 - Started two 5mL of E coli BL21 overnight - Designed procedure for applying mutagen and selecting for T7
5/20/13 - Performed T7 Mutagen Concentration Test - Performed T7 Minor Capsid Protein PCR
5/21/13 - Started two 5mL E coli BL21 overnight at around 7:00pm
5/22/13 - Performed spot test for 5.20 Mutagen Concentration Experiment - Ran agarose gel to confirm PCR product
5/23/13 - Started two 25mL E coli BL21 liquid culture over night at around 6:00pm
5/24/13 - Proceeded with 5.20 Mutagen Concentration Experiment by performing preliminary selection using x8 top agar
5/25/13 - Took pictures in preparation for Progress Report
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