Team:BYU Provo/Notebook/Metabolism/julyaug

From 2014.igem.org

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<blockquote><h2>Week of July 5th</h2></blockquote>
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<h2>Week of July 5th</h2>
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<blockquote><h3>June  30, 2014</h3></blockquote>
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<h3>June  30, 2014</h3>
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<blockquote><p>--BRK--I chose one colony of <i>E.coli</i> from four separate LB and CAM plates containing transformed bacteria with EreB and a promoter of either 101, 108, 111, or 119. These four colonies were streaked on four separate LB, CAM, and Erythromycin plates and grown overnight at 37C.</p></blockquote>
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<p>--BRK--I chose one colony of E.coli from four separate LB and CAM plates containing transformed bacteria with EreB and a promoter of either 101, 108, 111, or 119. These four colonies were streaked on four separate LB, CAM, and Erythromycin plates and grown overnight at 37C.</p>
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<blockquote><h3>July 1, 2014</h3></blockquote>
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<h3>July 1, 2014</h3>
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<blockquote><p>--BRK--The streaked colonies grew well on the LB/CAM/Erythromycin plates, indicating that the plasmid with the EreB gene had been successfully transformed. I took pictures of all the plates to compare the growth and use in the future to determine the effect of the different promoters.</p></blockquote>
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<p>--BRK--The streaked colonies grew well on the LB/CAM/Erythromycin plates, indicating that the plasmid with the EreB gene had been successfully transformed. I took pictures of all the plates to compare the growth and use in the future to determine the effect of the different promoters.</p>
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<blockquote><h3>July 3, 2014</h3></blockquote>
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<h3>July 3, 2014</h3>
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<blockquote><p>--BRK--Our team went to the wastewater treatment plant to learn more about the entire treatment process. I collected the biofilm and effluent water run-off from the plant to bring back to the lab for testing.</p></blockquote>
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<p>--BRK--Our team went to the wastewater treatment plant to learn more about the entire treatment process. I collected the biofilm and effluent water run-off from the plant to bring back to the lab for testing.</p>
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Revision as of 22:41, 23 July 2014


Week of July 5th

June 30, 2014

--BRK--I chose one colony of E.coli from four separate LB and CAM plates containing transformed bacteria with EreB and a promoter of either 101, 108, 111, or 119. These four colonies were streaked on four separate LB, CAM, and Erythromycin plates and grown overnight at 37C.

July 1, 2014

--BRK--The streaked colonies grew well on the LB/CAM/Erythromycin plates, indicating that the plasmid with the EreB gene had been successfully transformed. I took pictures of all the plates to compare the growth and use in the future to determine the effect of the different promoters.

July 3, 2014

--BRK--Our team went to the wastewater treatment plant to learn more about the entire treatment process. I collected the biofilm and effluent water run-off from the plant to bring back to the lab for testing.

Week of July 12th

Week of July 19th

Week of July 26th

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