Team:Calgary/28 May 2009
From 2009.igem.org
Revision as of 09:02, 21 August 2009 by Prima.moinul (Talk | contribs)
UNIVERSITY OF CALGARY
CAROL
Modeling Readings Continued
LuxCDABE-M-F:CCATTAATGAATTGCCGGATAATCTGGATTTTGAAGGCC LuxCDABE-M-R:GGCCTTCAAAATCCAGATTATCCGGCAATTCATTAATGG
|
CHINMOYEE
CLASS
|
EMILY
Sequencing of LuxOD47E in psB1AC3
File:2009.05.28.D47E BBkVer RD+PCR.tif
|
FAHD
Descriptive Title of What You're Doing
WIKI CODING HERE
|
IMAN
Descriptive Title of What You're Doing
WIKI CODING HERE
|
JAMIE
Descriptive Title of What You're Doing
WIKI CODING HERE
|
JEREMY
Send LuxO D47A in psB1AC3 Colony 2 to get sequenced
Although RD and PCR are effective means of verifying the presence of a sequence of DNA, the gold standard for verification is DNA sequencing. LuxO D47A in psB1AC3 Colony 2 was sent to the University of Calgary DNA Sequencing Facility (University Core DNA Services, Calgary, Alberta, Canada). Primers used were VF2 (anneals near the BBK prefix on the BBK vector - used as a forward primer) and VF1 (anneals near the BBK suffix on the BBK vector - used as a reverse primer). The template was prepared such that there was 100ng/1kb of DNA (gene of interest + vector).
After analyzing the sequencing results, it was evident that luxO D47A was absent from the psB1AC3 vector. |
KATIE
Descriptive Title of What You're Doing
WIKI CODING HERE
|
KEVIN
Matlab and symbiology
Familiarizing with the matlab program provided by MathWorks, and its biological tool called Symbiology.
No experiments were done on this day.
|
MANDY
Descriptive Title of What You're Doing
WIKI CODING HERE
|
PATRICK
Descriptive Title of What You're Doing
WIKI CODING HERE
|
PRIMA
Marketing
I spoke to the team about logos. We discussed logo ideas and designs. Also, I contacted the Gauntlet (U of C campus newsletter) about publishing a story on iGEM. I spoke to one of the Journalists and scheduled a meeting to interview some of my teammates.
|
STEFAN
Descriptive Title of What You're Doing
WIKI CODING HERE
|
VICKI
Gel electrophoresis of PCR and restriction digest products from yesterday
Purpose:
To analyse the PCR and restriction digest products from yesterday by running them on the gel. This will show:
Materials and methods:
Results: (insert May 28 gel picture here)
|