Team:British Columbia/Week2

From 2011.igem.org

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Monoterpene Synthase Project'''
 
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PsTPS-Pin:
 
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    Objective: PCR with designed primers for Site Directed Mutagenesis following the Stratagene Quikchange Protocol.
 
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    Procedures: Following the protocol from Stratagene Quikchange Protocol
 
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    Results: No PCR products were amplified after gel check with gel electrophoresis. Primers are visible on the gel.
 
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              Possible degradation of the Pfu polymerase, which explains why the PCR has not worked
 

Latest revision as of 05:35, 29 June 2011

Team: British Columbia - 2011.igem.org

Week 2: Monday May 9 - Sunday May 15

Contents

Monday

Dr. Joanne Fox begins a week of iGEM laboratory training in AMBL, the teaching lab in Michael Smith Laboratories. The training sessions run from 10am-4pm; Joanne provided short lectures so everyone understands the magic that goes on behind the actual bench work. Today, those present learned about restriction digests, and then set up restriction digests of the insert and vector in the morning. In the afternoon, we learned about purification kits, CIP assays, and ligation.

Tuesday

Wednesday

Marianne and Vicki (returning team members) went over labeling etiquette, lab book organization, and the 3-antibiotic method in the morning. In the afternoon, the team returned to AMBL to conduct transformation experiments on Monday's ligated parts.

Thursday

We did plate analysis, and started a culture for plasmid preps. Not everyone had colonies on their plates, so some had to steal others' colonies to start the culture.

In the afternoon, the team met up to discuss the pine beetle project in more detail - the objectives, the future applications/implications, the parts we need, the wet lab, modeling, and human practices components.

Friday

We mini-prepped the plasmids.

Saturday

Sunday