Team:WashU StLouis/Notebook/July

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<h1> <center><b> July</b> </center></h1>
<h1> <center><b> July</b> </center></h1>
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<td style="vertical-align: top;"><img
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style="width: 300px; height: 400px;" alt="Week 5"
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src="https://static.igem.org/mediawiki/2014/9/9b/WashU_Week_5.jpg"><br>
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</td>
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<td style="vertical-align: top;">
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<div style="text-align: center;"><span style="font-weight: bold;">Week
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Five- June 30- July 6</span><br>
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</div>
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Team starts re-culturing the strains in more nutritious LB media.&nbsp;
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Prepare 50% glycerol solution for storage and autoclaved water as well
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as the M9 medium. Caroline continues to work on scripts and outreach
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videos. Growth of all strains is significantly improved. <br>
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Brauer Group has not had success with chromophore plasmid yet,
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redesigned the plasmid by piecing together different components.
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Started with cloning of proposed hybrid promoter and sent in for
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sequence verification.<br>
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Had our third worldly Wednesday at Gyro House- Mediterranean cuisine. </td>
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<td style="vertical-align: top;"><img
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style="width: 300px; height: 405px;" alt="Week 6"
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src="https://static.igem.org/mediawiki/2014/8/88/WashU_Week_6.jpg"><br>
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</td>
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<td style="vertical-align: top;">
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<div style="text-align: center;"><span style="font-weight: bold;">Week
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Six- July 7-13</span><br>
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</div>
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After series of culturing testing, the best media, optimal nitrogen
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source, optimal carbon source, optimal temperature for culturing are
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all determined. C-source: Glucose. N-source: Glutamate. Culturing
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Media: LB. Testing Media: M9. Temperature: 30 Celsius (Anaerobic).
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&nbsp;<br>
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Brauer group continued work on chromophore plasmid. Started design of
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experimentation without the chromophore as a sanity check. Ptet
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promoter seemed to be giving our plasmids issues as it did not
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fluoresce as expected. Contacted Tabor group for possibly shipping the
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plasmid to WashU.<br>
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Had a mid summer progress report meeting with the professors and
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explained to them our work’s progress and difficulties we faced.<br>
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Had our fourth Worldly Wednesday at Asian Kitchen- Korean cuisine.</td>
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<td style="vertical-align: top;"><img
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style="width: 300px; height: 400px;" alt="Week 7 picture"
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src="https://static.igem.org/mediawiki/2014/a/af/WashU_Week_7.jpg"><br>
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</td>
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<td style="vertical-align: top;">
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<div style="text-align: center;"><span style="font-weight: bold;">Week
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Seven- July 14-20</span><br>
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</div>
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Before the formal examination (Acetylene Reduction Assay) for the
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nitrogenase activity, the team performed plasmid extraction and gel
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running to confirm the existence of plasmid inside the strains. <br>
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Brauer Group worked on cloning for degradation tags and other side
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projects. Continued conversations with shipping plasmid to WashU and
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also found a promising Biobrick part and ordered from the registry. <br>
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Ben started working on a math model of our system with Brandon.<br>
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</td>
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<td style="vertical-align: top;"><img
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style="width: 300px; height: 405px;" alt="Week 8 picture"
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src="https://static.igem.org/mediawiki/2014/2/2c/WashU_Week_8.jpg"><br>
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</td>
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<td style="vertical-align: top;">
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<div style="text-align: center;"><span style="font-weight: bold;">Week
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Eight- July 21-27</span><br>
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</div>
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Rebstock group ran the Acetylene Reduction Assay with GC machine for
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all strains including negative control. Specific procedure can be found
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in protocol. <br>
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Brauer group received the biobrick part and started cloning a new
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plasmid for the chromophore part, and sent in for sequencing.<br>
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Ben continued work on math model with Brandon by sending necessary
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information to him and writing ODEs.<br>
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The team had our fifth worldly Wednesday at De Palm Tree- Jamaican
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cuisine… spicy!!<br>
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</td>
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</tr>
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<td style="vertical-align: top;"><img
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style="width: 300px; height: 493px;" alt="Week 9 pic"
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src="https://static.igem.org/mediawiki/2014/e/e3/WashU_Week9.jpg"><br>
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</td>
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<td style="vertical-align: top;">
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<div style="text-align: center;"><span style="font-weight: bold;">Week
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Nine- July 28- August 3</span><br>
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</div>
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Continued Acetylene Reduction Assays for all strains and controls. <br>
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Brauer group continued troubleshooting of chromophore plasmid. And sent
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off degradation tag plasmids for sequencing as well. Designed an
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experiment for light induction by co-transforming chromophore plasmids
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and light regulation plasmids. Make necessary plates for experiment and
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started growing cultures for experimentation.</td>
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</table>
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Revision as of 21:42, 26 September 2014