Team:British Columbia/Notebook/27 June 2011

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==June 27 2011==
==June 27 2011==

Revision as of 22:37, 3 July 2011

Team: British Columbia - 2011.igem.org

Contents

June 27 2011

We created a set of lab rules due to common mistakes made in the lab over the past few weeks.

Vicki and Marianne will having training sessions throughout the week to show team members without much wetlab experience how to PCR, cast and run a gel, digest, ligate, transform, design primers, send miniprepped products to be sequenced.

Competent cells - tested, and they're competent! Good job Gurpal and Sam!

Modeling: Jacob obtained the ARC program. Gurpal wants to create a wetlab flow chart to match the modeling.

Sent DspB (part from last year) to Grinnell College (a new iGEM team this year who requested our part) in the United States.

alpha-pinene synthase

  • SDM-PCR worked! (Used the QuikChange SDM Kit protocol).

3-carene synthase

Daisy needs to make custom primers for sequencing purposes because the mutagen site is in the middle of the coding sequence and her flanking primers will only sequence 700-800bp into the sequence.

beta-pinene synthase

  • Resuspended SDM forward and reverse primers

(-)-limonene synthase

  • Resuspended SDM forward and reverse primers
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