Team:UQ-Australia/Notebook/June
From 2011.igem.org
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- | + | |rowspan="2"|In this period of time we continued to work on the cloning of our parts, where we encountered a number of issues. We also conducted a number of outreach activities, such as the Biofutures camp, and began work on an analysis of patent practices and how this relates to iGEM's registry. | |
- | + | ! [[File:UQ-Australia_logo_2011.png|125x125px|link=https://2011.igem.org/Team:UQ-Australia]] | |
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+ | == '''<span style="color:#558822"> Summary of Lab Work </span>''' == | ||
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+ | We ligated araC and pBAD into the iGEM plasmid backbone. However, after transforming them parts and then miniprepping them we found that the ligation was not successful. | ||
- | + | We re-suspended a number of parts from the iGEM distribution kit, including LacI, GFP and pSB3K3 plasmid backbone. | |
- | + | These parts were transformed, as were some other genes we had synthesized. We also transformed more of the pSB1C3 plasmid backbone. | |
- | == | + | Minipreps were done of the transformations of GFP, lacI, Plac/ara, GlnAp2. Nanodrop of the final concentrations: |
+ | GFP = 46.6ng/ul | ||
+ | LacI = 40.8ng/ul | ||
+ | Plac/ara = 81.6ng/ul | ||
+ | GlnAp2 = 54.4ng/ul | ||
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- | + | 3ml culture of the pSB1C3 transformations was prepared, followed by miniprep. Nandrop = 94.9ng/ul |
Latest revision as of 00:44, 6 October 2011