Team:WashU StLouis/Notebook/July
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<h1> <center><b> July</b> </center></h1> | <h1> <center><b> July</b> </center></h1> | ||
- | + | <div style="text-align: center;"> | |
- | < | + | <h3><a href="https://2014.igem.org/Team:WashU_StLouis/Notebook">Notebook</a> |
- | + | | <a | |
+ | href="https://2014.igem.org/Team:WashU_StLouis/Notebook/June">June</a> | ||
+ | | <a | ||
+ | href="https://2014.igem.org/Team:WashU_StLouis/Notebook/August">August</a> | ||
+ | | <a href="https://2014.igem.org/Team:WashU_StLouis/Notebook/September">School Year</a></h3> | ||
+ | </div> | ||
+ | <center> <img style="border: 0px solid ; width: 100%;" alt="July Calendar" src="https://static.igem.org/mediawiki/2014/e/e1/WashU_July_Calendar.png"> </center> <br><br> | ||
+ | <body> | ||
+ | <br> | ||
+ | <table | ||
+ | style="text-align: left; width: 80%; height: 1300px; margin-left: auto; margin-right: auto;" | ||
+ | border="1" cellpadding="5" cellspacing="0"> | ||
+ | <tbody> | ||
+ | <tr> | ||
+ | <td style="vertical-align: top;"><img | ||
+ | style="width: 300px; height: 400px;" alt="Week 5" | ||
+ | src="https://static.igem.org/mediawiki/2014/9/9b/WashU_Week_5.jpg"><br> | ||
+ | </td> | ||
+ | <td style="vertical-align: top;"> | ||
+ | <div style="text-align: center;"><span style="font-weight: bold;">Week | ||
+ | Five- June 30- July 6</span><br> | ||
+ | </div> | ||
+ | Team starts re-culturing the strains in more nutritious LB media. | ||
+ | Prepare 50% glycerol solution for storage and autoclaved water as well | ||
+ | as the M9 medium. Caroline continues to work on scripts and outreach | ||
+ | videos. Growth of all strains is significantly improved. <br> | ||
+ | Brauer Group has not had success with chromophore plasmid yet, | ||
+ | redesigned the plasmid by piecing together different components. | ||
+ | Started with cloning of proposed hybrid promoter and sent in for | ||
+ | sequence verification.<br> | ||
+ | Website worked on compiling notebook and log information. <br> | ||
+ | Had our third worldly Wednesday at Gyro House- Mediterranean cuisine. </td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td style="vertical-align: top;"><img | ||
+ | style="width: 300px; height: 405px;" alt="Week 6" | ||
+ | src="https://static.igem.org/mediawiki/2014/8/88/WashU_Week_6.jpg"><br> | ||
+ | </td> | ||
+ | <td style="vertical-align: top;"> | ||
+ | <div style="text-align: center;"><span style="font-weight: bold;">Week | ||
+ | Six- July 7-13</span><br> | ||
+ | </div> | ||
+ | After series of culturing testing, the best media, optimal nitrogen | ||
+ | source, optimal carbon source, optimal temperature for culturing are | ||
+ | all determined. C-source: Glucose. N-source: Glutamate. Culturing | ||
+ | Media: LB. Testing Media: M9. Temperature: 30 Celsius (Anaerobic). | ||
+ | <br> | ||
+ | Brauer group continued work on chromophore plasmid. Started design of | ||
+ | experimentation without the chromophore as a sanity check. Ptet | ||
+ | promoter seemed to be giving our plasmids issues as it did not | ||
+ | fluoresce as expected. Contacted Tabor group for possibly shipping the | ||
+ | plasmid to WashU.<br> | ||
+ | Website created footer along with sponsors banner.<br> | ||
+ | Had a mid summer progress report meeting with the professors and | ||
+ | explained to them our work's progress and difficulties we faced.<br> | ||
+ | Had our fourth Worldly Wednesday at Asian Kitchen- Korean cuisine.</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td style="vertical-align: top;"><img | ||
+ | style="width: 300px; height: 400px;" alt="Week 7 picture" | ||
+ | src="https://static.igem.org/mediawiki/2014/a/af/WashU_Week_7.jpg"><br> | ||
+ | </td> | ||
+ | <td style="vertical-align: top;"> | ||
+ | <div style="text-align: center;"><span style="font-weight: bold;">Week | ||
+ | Seven- July 14-20</span><br> | ||
+ | </div> | ||
+ | Before the formal examination (Acetylene Reduction Assay) for the | ||
+ | nitrogenase activity, the team performed plasmid extraction and gel | ||
+ | running to confirm the existence of plasmid inside the strains. <br> | ||
+ | Brauer Group worked on cloning for degradation tags and other side | ||
+ | projects. Continued conversations with shipping plasmid to WashU and | ||
+ | also found a promising Biobrick part and ordered from the registry. <br> | ||
+ | Website start to incorporate videos onto the site. <br> | ||
+ | Ben also started working on a math model of our system with Brandon.<br> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td style="vertical-align: top;"><img | ||
+ | style="width: 300px; height: 405px;" alt="Week 8 picture" | ||
+ | src="https://static.igem.org/mediawiki/2014/2/2c/WashU_Week_8.jpg"><br> | ||
+ | </td> | ||
+ | <td style="vertical-align: top;"> | ||
+ | <div style="text-align: center;"><span style="font-weight: bold;">Week | ||
+ | Eight- July 21-27</span><br> | ||
+ | </div> | ||
+ | Rebstock group ran the Acetylene Reduction Assay with GC machine for | ||
+ | all strains including negative control. Specific procedure can be found | ||
+ | in protocol. <br> | ||
+ | Brauer group received the biobrick part and started cloning a new | ||
+ | plasmid for the chromophore part, and sent in for sequencing.<br> | ||
+ | Ben continued work on math model with Brandon by sending necessary | ||
+ | information to him and writing ODEs.<br> | ||
+ | Website worked on formatting layout. Added floating menu to certain pages. Created front page for deadlines <br> | ||
+ | The team had our fifth worldly Wednesday at De Palm Tree- Jamaican | ||
+ | cuisine... spicy!!<br> | ||
+ | </td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td style="vertical-align: top;"><img | ||
+ | style="width: 300px; height: 493px;" alt="Week 9 pic" | ||
+ | src="https://static.igem.org/mediawiki/2014/e/e3/WashU_Week9.jpg"><br> | ||
+ | </td> | ||
+ | <td style="vertical-align: top;"> | ||
+ | <div style="text-align: center;"><span style="font-weight: bold;">Week | ||
+ | Nine- July 28- August 3</span><br> | ||
+ | </div> | ||
+ | Continued Acetylene Reduction Assays for all strains and controls. <br> | ||
+ | Brauer group continued troubleshooting of chromophore plasmid. And sent | ||
+ | off degradation tag plasmids for sequencing as well. Designed an | ||
+ | experiment for light induction by co-transforming chromophore plasmids | ||
+ | and light regulation plasmids. Make necessary plates for experiment and | ||
+ | started growing cultures for experimentation.<br> | ||
+ | Website started adding content to the various pages </td> | ||
+ | </tr> | ||
+ | </tbody> | ||
+ | </table> | ||
+ | <br> | ||
+ | <br> | ||
+ | <br> | ||
+ | </body> | ||
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Latest revision as of 22:15, 17 October 2014
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