Difference between revisions of "Team:HK SSC/Collaborations"

 
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<h1>Collaborations</h1>
 
<h1>Collaborations</h1>
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Sharing and collaboration are core values of iGEM. We encourage you to reach out and work with other teams on difficult problems that you can more easily solve together.
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<h3>Silver Medal Criterion #2</h3>
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Document your collaboration(s) clearly on this page to compete for the silver medal criterion #2 on collaboration. Please see the <a href="https://2019.igem.org/Judging/Medals">2019 Medals Page</a> for more information.
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<h4> Which other teams can we work with? </h4>
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style='mso-spacerun:yes'>&nbsp;</span></span></p>
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You can work with any other team in the competition, including standard, software, open, and high school track teams. You can also work with non-iGEM research groups, but they do not count towards the iGEM team collaboration silver medal criterion.
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<h3>SZTA_Szeged_HU</h3>
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In order to meet the silver medal criteria on helping another team, you must complete this page and detail the nature of your collaboration with another iGEM team.
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<p>With similar objectives on our projects, we are honoured to be able to collaborate with team SZTA_Szeged_HU. Their project aims to detect Microcystin toxin in waters using bioindicators. </br>
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<div class="center"><img style="width:60%; height:60%; margin: auto;" src="https://static.igem.org/mediawiki/2019/4/47/T--HK_SSC--image1.jpeg"/></div>
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<div class="center"><b>Fig1. Team SZTA_Szeged_HU</b></div>
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<p>Here are some areas we collaborated on: </p>
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<h4>1. Providing us with their plasmid </h4>
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<p>Team SZTA_Szeged_HU has designed 2 plasmids for the detection of Microcystin toxin. Since our project aims to remove Microcystin, they provided us with their plasmids, so that we can conduct further detailed downstream analysis. In return, we will be giving them our experimental data. </p>
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Here are some suggestions for projects you could work on with other teams:
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<div class="center"><img style="width:60%; height:60%; margin: auto;" src="https://static.igem.org/mediawiki/2019/c/c0/T--HK_SSC--Hungary_gel_pic.png"/></div>
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<div class="center"><b>Fig2. Showing the correct band sizes of the plasmids provided by SZTA_Szeged_HU. The expected band size is around 3800bp. (Circular plasmid DNA often shows smaller band size than expected)</b></div>
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<div class="center"><img style="width:40%; height:40%; margin: auto;" src="https://static.igem.org/mediawiki/2019/f/fd/T--HK_SSC--Collab_plate1_equation.png"/></div>
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<div class="center"><b>Fig3. Successful transfromation of the 2 plasmid constructs</b></div></br>
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<p>However, we failed to excite the green fluorescent  protein in the diluted overnight cultures, possibly due to wrong wavelength (the GFP used in our project is different from that of team SZTA_Szeged_HU). We have refelected the experiment results. </p>
  
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<li> Improve the function of another team's BioBrick Part or Device</li>
 
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<li> Characterize another team's part </li>
 
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<li> Debug a construct </li>
 
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<li> Model or simulate another team's system </li>
 
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<li> Test another team's software</li>
 
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<li> Help build and test another team's hardware project</li>
 
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<li> Mentor a high-school team</li>
 
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<h4>2. Survey </h4>
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<p>We helped them collect data for their surveys. These surveys include interviewing fishpond owners and researchers about how algal blooms have affected them. </p>
 
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Latest revision as of 02:15, 22 October 2019

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Collaborations

 

SZTA_Szeged_HU

With similar objectives on our projects, we are honoured to be able to collaborate with team SZTA_Szeged_HU. Their project aims to detect Microcystin toxin in waters using bioindicators.

Fig1. Team SZTA_Szeged_HU


Here are some areas we collaborated on:


1. Providing us with their plasmid

Team SZTA_Szeged_HU has designed 2 plasmids for the detection of Microcystin toxin. Since our project aims to remove Microcystin, they provided us with their plasmids, so that we can conduct further detailed downstream analysis. In return, we will be giving them our experimental data.

Fig2. Showing the correct band sizes of the plasmids provided by SZTA_Szeged_HU. The expected band size is around 3800bp. (Circular plasmid DNA often shows smaller band size than expected)
Fig3. Successful transfromation of the 2 plasmid constructs

However, we failed to excite the green fluorescent protein in the diluted overnight cultures, possibly due to wrong wavelength (the GFP used in our project is different from that of team SZTA_Szeged_HU). We have refelected the experiment results.


2. Survey

We helped them collect data for their surveys. These surveys include interviewing fishpond owners and researchers about how algal blooms have affected them.