Team:Calgary/5 August 2009
From 2009.igem.org
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<i>Pqrr4</i>+B0034+K082003 was isolated in order to verify its presence using Restriction digest and Sequencing later on. The product's purity and concentration were measured using Nanodrop utility and spectrophotometer. | <i>Pqrr4</i>+B0034+K082003 was isolated in order to verify its presence using Restriction digest and Sequencing later on. The product's purity and concentration were measured using Nanodrop utility and spectrophotometer. | ||
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| ''Pqrr4''+B0034+K082003 C9 #2|| 2.06 || 3.61 || 160.4 | | ''Pqrr4''+B0034+K082003 C9 #2|| 2.06 || 3.61 || 160.4 | ||
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Restriction digest on <i>Pqrr4</i>+B0034+K082003 to verify its presence. This is our reporter circuit. The product was ran on 1.5% gel at 90V. | Restriction digest on <i>Pqrr4</i>+B0034+K082003 to verify its presence. This is our reporter circuit. The product was ran on 1.5% gel at 90V. | ||
[[Image:Calgary_2009.08.05.Pqrr4%2BB0034%2BK082003.png|700px]] | [[Image:Calgary_2009.08.05.Pqrr4%2BB0034%2BK082003.png|700px]] | ||
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+ | Yesterday, I have done an overnight digestion of <i>Pqrr4</i>+I13500 and Q04510 (inverter) part in pSB2K3 vector. Today, with this product, I have performed phophatase treatment on Q04510 and ligated them together. This product was then transformed into TOP10 cells, and is now growing in the incubator at 37˚C. | ||
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Revision as of 21:56, 5 August 2009
UNIVERSITY OF CALGARY