Difference between revisions of "Team:Uniandes Colombia/Attributions"

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<h2> Attributions</h2>
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<b><font color="#8A0808" size="5" >Attributions</font></b>
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<p> Each team must clearly attribute work done by the student team members on this page. The team must distinguish work done by the students from work done by others, including the host labs, advisors, instructors, and individuals not on the team roster. </p>
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<h4> Can we base our project on a previous one? </h4>
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<p>Yes! You can have a project based on a previous team, or based on someone else's idea, <b>as long as you state this fact very clearly and give credit for the original project.</b> </p>
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<h4> Why is this page needed? </h4>
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<p>The Attribution requirement helps the judges know what you did yourselves and what you had help with. We don't mind if you get help with difficult or complex techniques, but you must report what work your team did and what work was done by others.</p>
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For example, you might choose to work with an animal model during your project. Working with animals requires getting a license and applying far in advance to conduct certain experiments in many countries. This is difficult to achieve during the course of a summer, but much easier if you can work with a postdoc or PI who has the right licenses.</p>
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Our proposal is to create a system which allows us to measure a biological signal precisely and without delay. But we are not the first who make this kind of attempt. In 2008 Harvard iGem team developed a similar idea: they introduce a plasmid into Shewanella oneidensis which contain a Lac promoter  coupled with gene that codifies to mtrB cytochrome.  The last protein belongs to an oxidation complex that reduces minerals by electron transference. Hence, Shewanella produced an electrical signal when stimulated with lactose.
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<h5> What should this page have?</h5>
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On the other hand, Chile 2012 coupled a bioluminescent molecule to the circadian clock of cyanobacteria. Their aim was to produce a bioluminescent cyanobacteria which lights up during dusk hours and regenerates the substrates during the day.
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<li>General Support</li>
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<li>Project support and advice</li>
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<li>Fundraising help and advice</li>
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<li>Lab support</li>
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<li>Difficult technique support</li>
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<li>Project advisor support</li>
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<li>Wiki support</li>
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<li>Presentation coaching</li>
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<li>Human Practices support</li>
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<li> Thanks and acknowledgements for all other people involved in helping make a successful iGEM team</li>
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<h4>Inspiration</h4>
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<p>Take a look at what other teams have done:</p>
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<li><a href="https://2011.igem.org/Team:Imperial_College_London/Team">2011 Imperial College London</a> (scroll to the bottom)</li>
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<li><a href="https://2014.igem.org/Team:Exeter/Attributions">2014 Exeter </a></li>
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<li><a href="https://2014.igem.org/Team:Melbourne/Attributions">2014 Melbourne </a></li>
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<li><a href="https://2014.igem.org/Team:Valencia_Biocampus/Attributions">2014 Valencia Biocampus</a></li>
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Revision as of 03:56, 19 September 2015

iGEM Uniandes-Colombia

Team Project Wet Lab Dry Lab Hardware Human Practices Collaborations -
Attributions

Our proposal is to create a system which allows us to measure a biological signal precisely and without delay. But we are not the first who make this kind of attempt. In 2008 Harvard iGem team developed a similar idea: they introduce a plasmid into Shewanella oneidensis which contain a Lac promoter coupled with gene that codifies to mtrB cytochrome. The last protein belongs to an oxidation complex that reduces minerals by electron transference. Hence, Shewanella produced an electrical signal when stimulated with lactose.

On the other hand, Chile 2012 coupled a bioluminescent molecule to the circadian clock of cyanobacteria. Their aim was to produce a bioluminescent cyanobacteria which lights up during dusk hours and regenerates the substrates during the day.