Team:DTU Denmark/notebookredoxilator

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Revision as of 20:37, 21 October 2009 by Kaas (Talk | contribs)

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Welcome to the DTU iGEM wiki!


Activities relating to our two sub-projects:

- The Redoxilator
- The USERTM assembly standard
- Biobricks
- Protocols

Day-to-day activities


Activities relating to the redoxilator

Thursday 15/10/2009
BioLector experiment initiated! Lets get some results!

Wednesday 14/10/2009
Colonies were picked from plate to grow to have inoculum for the BioLector experiment tomorrow

Monday 5/10/2009
Yeast streak diluted to new plate to be sure we have a real transformant

Thursday 1/10/2009
Construt and Leaky are ready for yeast transformation into CEN PK 113 5D (Ura-) using the URA marker on these plasmidss

Wednesday 30/9/2009
Purification of vector. Digestion with XmaI of leaky p241i was conducted (Should yield 2500 & 4500)

Tuesday 29/9/2009
Liquid over night colonies. Cultures were randomly picked using a sterile pipette tip from the transformation plate and incubated into liquid media containing kanamycin.

Monday 28/9/2009
The construct AKA p241i digested wiith NotI to remove the redoxilated. Following gelpurification the backbone with ligated and transformed into E coli

Friday 25/9/2009
Colonies seen!

Thursday 24/9/2009
Our dear redoxilator construct arrieved from California (DNA 2.0) Dna extracted from filter paper and transformed into E Coli
Work process

Our team works parallel in smaller sub-teams. Some of us work hard in the lab, while others are in the process of developing software and the in silico model of the Redoxilator system. However, we constantly keep each other updated, and meet often to exchange ideas and take turns at the different tasks, thus exhausting all of our combined knowledge in every aspect of this project.

Comments or questions to the team? Please -- Comments of questions to webmaster? Please