Team:BostonU/NotebookQS

From 2013.igem.org

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<p>Today, we did Phusion PCR using the genomic DNA of Chomobacterium violaceum as the template for the CviI and CviR systems.  We ran the PCR product on a gel and the CviI did not appear on the gel.  The CviR system appeared and we gel extracted the parts.</p>
<p>Today, we did Phusion PCR using the genomic DNA of Chomobacterium violaceum as the template for the CviI and CviR systems.  We ran the PCR product on a gel and the CviI did not appear on the gel.  The CviR system appeared and we gel extracted the parts.</p>
<p>The gel concentrations are as follows:</p>
<p>The gel concentrations are as follows:</p>
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<th>Sample</th>
<th>Sample</th>
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<td>-28.27</td>
<td>-28.27</td>
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Revision as of 16:53, 22 July 2013



Quorum Sensing Notebook

June 2013

We planned out that we will transform E. coli with the civI/civR system found in Chromobacterium violaceum. We will design MoClo devices that include these systems. In the meantime, we are beginning to design primers that will make the civI/civR system into a MoClo system by adding the the fusion site in addition to the BBS and SpeI sites. Then, we will develop a PCR strategy.


June 18, 2013

Our advisor, Traci, emailed different labs and PIs that work with Chromobacterium violaceum. Dr. Jim Thoden from the Holden Lab at the University of Wisconsin sent us genomic DNA.


June 20, 2013

We designed forward and reverse primers for CviR/CviI systems and ordered those primers. We are currently waiting on acquiring the primers to begin PCR.


July 8, 2013

Today, we did Phusion PCR using the genomic DNA of Chomobacterium violaceum as the template for the CviI and CviR systems. We ran the PCR product on a gel and the CviI did not appear on the gel. The CviR system appeared and we gel extracted the parts.

The gel concentrations are as follows:

Sample ng/µL 260/280 260/230
CviR_CD - A 1.6 1.29 0.01
CviR_CD - B 5.4 4.48 -28.27