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Team:Calgary/14 July 2010
From 2010.igem.org
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Today I Gen-Elute Mini Prepared 8 tubes of I0500+E0034+E0040 from 4 different colonies and 4 tubes of plasmid switched K239000 and K135000. I then constructed K239000 with I13507 and I13504, then K135000 with I13507 and I13504. | Today I Gen-Elute Mini Prepared 8 tubes of I0500+E0034+E0040 from 4 different colonies and 4 tubes of plasmid switched K239000 and K135000. I then constructed K239000 with I13507 and I13504, then K135000 with I13507 and I13504. | ||
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<u>Himika</u> | <u>Himika</u> | ||
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Strategy II: This involves similar process but instead this would introduce cloning sites on the outside of the gene as well. The reason for introducing the arbitrary cloning sites on the outside of the circuit is to allow us to clone in the whole circuit in the Biobrick vector much more easily. | Strategy II: This involves similar process but instead this would introduce cloning sites on the outside of the gene as well. The reason for introducing the arbitrary cloning sites on the outside of the circuit is to allow us to clone in the whole circuit in the Biobrick vector much more easily. | ||
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<u>Team</u> | <u>Team</u> | ||
Revision as of 15:43, 20 July 2010
Notebook
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Notebook
No notebook page exists for this date. Sorry!
Retrieved from "http://2010.igem.org/Team:Calgary/14_July_2010"
