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Team:Calgary
From 2010.igem.org
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| - | div.blueBox img, | + | div.blueBox img, #greenBox1 img, #greenBox2 img, #greenBox3 img, div.purpleBox img{ |
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margin-left: 5px; | margin-left: 5px; | ||
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| - | div.blueBox p, | + | div.blueBox p, #greenBox1 p, #greenBox2 p, #greenbox3 p, div.purpleBox p{ |
clear: left; | clear: left; | ||
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background-color: #54bcf8; | background-color: #54bcf8; | ||
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| + | div.blueBox p a{ | ||
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| + | font-weight:bold; | ||
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<div class="miniContainer"> | <div class="miniContainer"> | ||
| - | <img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/RecentPhotosTab.png" class="galleryButton"></img> | + | <a href="https://2010.igem.org/Team:Calgary/Community/Gallery"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/RecentPhotosTab.png" class="galleryButton"></img></a> |
| - | <img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/SponsoroftheMonthButton.png" class="sponsorButton"></img> | + | <a href="https://2010.igem.org/Team:Calgary/Sponsors"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/SponsoroftheMonthButton.png" class="sponsorButton"></img></a> |
</div> | </div> | ||
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<div class="twitterTicker"> | <div class="twitterTicker"> | ||
<img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Twitter.png"></img> | <img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Twitter.png"></img> | ||
| - | <iframe src="http://s1.rsspump.com/rss.aspx?s=a65f65cb-5561-4e09-ab23- | + | <iframe src="http://s1.rsspump.com/rss.aspx?s=a65f65cb-5561-4e09-ab23-1b518cb1b35e&speed=1&t=0&d=1&u=0&p=0&b=0&ic=5&font=Verdana&fontsize=12px&bgcolor=&color=000000&type=typewriter&su=0&sub=0&sw=0" frameborder="0" width="100%" height="16" scrolling="no" allowtransparency="true"></iframe><noframes><div style="background-color: none transparent;"><a href="http://www.rsspump.com/?web_widget/rss_widget/twitter_widget" title="web widget">Twitter Widget</a></div></noframes> |
| - | + | ||
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| - | + | ||
| - | + | ||
| - | style="background-color: none transparent;"><a href="http://www.rsspump.com/?web_widget/rss_widget/twitter_widget" title="web widget">Twitter | + | |
| - | + | ||
| - | Widget</a></div></noframes> | + | |
<p><a href="http://twitter.com/iGEMCalgary">Follow us on Twitter!</a></p> | <p><a href="http://twitter.com/iGEMCalgary">Follow us on Twitter!</a></p> | ||
</div> | </div> | ||
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<div class="blueBox"> | <div class="blueBox"> | ||
<img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Modellingtxt.png"></img> | <img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Modellingtxt.png"></img> | ||
| - | <p>Our modelling project | + | <p>Our modelling project consists of two components: a mathematical model done in MATLAB and an animation done in Autodesk <i>Maya</i>. We hope to model the formation of inclusion bodies, which are aggregations of misfolded protein that can occur within cells. |
| + | You can click <a href="https://2010.igem.org/Team:Calgary/Modelling">here</a> to read more about our modelling project.</p> | ||
</div> | </div> | ||
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<div class="greenContainer"> | <div class="greenContainer"> | ||
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<img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Circuit1.png"></img> | <img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Circuit1.png"></img> | ||
<p>Description of Circuit 1 goes here.</p> | <p>Description of Circuit 1 goes here.</p> | ||
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<img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Circuit2.png"></img> | <img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Circuit2.png"></img> | ||
<p>Description of Circuit 2 goes here.</p> | <p>Description of Circuit 2 goes here.</p> | ||
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<img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Circuit3.png"></img> | <img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/Circuit3.png"></img> | ||
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<div class="purpleBox"> | <div class="purpleBox"> | ||
<img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/NewsFeed.png"></img> | <img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/NewsFeed.png"></img> | ||
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<div class="projectDescContainer"> | <div class="projectDescContainer"> | ||
| - | <img class="descTitle" title="Project Description" | + | <img class="descTitle" title="Project Description" src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/ProjectDescription.png"></img> |
| - | + | <p>Many synthetic biology projects involve the expression of recombinant proteins in microorganisms such as E. coli. The problems encountered with many synthetic biology projects often involve problems with protein expression. It is often very difficult to recognize the problem and pinpoint where it lies. The goal of the University of Calgary 2010 iGEM team is to build a protein expression "troubleshooting kit". This kit will contain two systems with which target genes can be inserted. In the resulting cell growth, fluorescent protein production will be used to determine whether there is a problem with protein expression as well as indicate where the protein expression is failing.</p> | |
| - | src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/ProjectDescription.png"></img> | + | <p>Protein expression happens in three steps: the transcription of the DNA to mRNA, the translation of mRNA into an amino acid sequence, and the folding of that amino acid sequence into a protein. Our system detects possible errors in these three steps using two circuits. The first circuit has a fluorescent reporter that is produced when DNA is transcribed into mRNA and another that is produced when mRNA is translated into a functional protein. When both reporter proteins are expressed in the cell, it indicates both transcription and translation are successful. The second circuit involves reporter systems that are activated as a result of protein misfolding. Two native stress-activated promoters from E. coli were engineered upstream to fluorescent reporters that will respond to periplasmic and cytoplasmic protein misfolding. If the protein of interest misfolds in either area of the cell, one of the promoters will be activated and the corresponding fluorescence will be observed.</p> |
| - | <p>Many synthetic biology projects involve the expression of recombinant proteins in microorganisms such as E. coli. The problems | + | |
| - | + | ||
| - | encountered with many synthetic biology projects often involve problems with protein expression. It is often very difficult to recognize the | + | |
| - | + | ||
| - | problem and pinpoint where it lies. The goal of the University of Calgary 2010 iGEM team is to build a protein expression "troubleshooting kit". | + | |
| - | + | ||
| - | This kit will contain two systems with which target genes can be inserted. In the resulting cell growth, fluorescent protein production will be | + | |
| - | + | ||
| - | used to determine whether there is a problem with protein expression as well as indicate where the protein expression is failing.</p> | + | |
| - | <p>Protein expression happens in three steps: the transcription of the DNA to mRNA, the translation of mRNA into an amino acid | + | |
| - | + | ||
| - | sequence, and the folding of that amino acid sequence into a protein. Our system detects possible errors in these three steps using two circuits. | + | |
| - | + | ||
| - | The first circuit has a fluorescent reporter that is produced when DNA is transcribed into mRNA and another that is produced when mRNA is | + | |
| - | + | ||
| - | translated into a functional protein. When both reporter proteins are expressed in the cell, it indicates both transcription and translation are | + | |
| - | + | ||
| - | successful. The second circuit involves reporter systems that are activated as a result of protein misfolding. Two native stress-activated | + | |
| - | + | ||
| - | promoters from E. coli were engineered upstream to fluorescent reporters that will respond to periplasmic and cytoplasmic protein misfolding. If | + | |
| - | + | ||
| - | the protein of interest misfolds in either area of the cell, one of the promoters will be activated and the corresponding fluorescence will be | + | |
| - | + | ||
| - | observed.</p> | + | |
<p><a href="https://2010.igem.org/Team:Calgary/Project">Read more...</a></p> | <p><a href="https://2010.igem.org/Team:Calgary/Project">Read more...</a></p> | ||
</div> | </div> | ||
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<table> | <table> | ||
<tr> | <tr> | ||
| - | <td><a href="#"><img src="http://www.sciencemediacentre.ca/smc/images/stories/logos/AI% | + | <td><a href="#"><img src="http://www.sciencemediacentre.ca/smc/images/stories/logos/AI%20Tech_RGB.jpg"></img></a></td> |
| - | + | ||
| - | 20Tech_RGB.jpg"></img></a></td> | + | |
<td><a href="#"><img src="http://enel.ucalgary.ca/mitacs/MITACS/images/Logo_UofC.jpg"></img></a></td> | <td><a href="#"><img src="http://enel.ucalgary.ca/mitacs/MITACS/images/Logo_UofC.jpg"></img></a></td> | ||
<td><a href="#"><img src="https://static.igem.org/mediawiki/2008/7/7b/Bioalberta.jpeg"></img></a></td> | <td><a href="#"><img src="https://static.igem.org/mediawiki/2008/7/7b/Bioalberta.jpeg"></img></a></td> | ||
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<tr> | <tr> | ||
<td><a href="#"><img src="http://www.innolution.com/img/autodesk_logo.jpg"></img></a></td> | <td><a href="#"><img src="http://www.innolution.com/img/autodesk_logo.jpg"></img></a></td> | ||
| - | <td><a href="#"><img | + | <td><a href="#"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/NEB_logoSmall2.png"></img></a></td> |
| - | + | <td><a href="#"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/VWRLogoCallBlue-HIGHREScopy2.png"></img></a></td> | |
| - | src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/NEB_logoSmall2.png"></img></a></td> | + | |
| - | <td><a href="#"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/VWRLogoCallBlue- | + | |
| - | + | ||
| - | HIGHREScopy2.png"></img></a></td> | + | |
</tr> | </tr> | ||
<tr> | <tr> | ||
| - | <td><a href="#"><img | + | <td><a href="#"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/bhsgrnsmall.png"></img></a></td> |
| - | + | ||
| - | src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/bhsgrnsmall.png"></img></a></td> | + | |
<td><a href="#"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/AHFMRlogo.png"></img></a></td> | <td><a href="#"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/AHFMRlogo.png"></img></a></td> | ||
<td><a href="#"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/IDTLogo.png"></img></a></td> | <td><a href="#"><img src="http://i872.photobucket.com/albums/ab287/iGEMCalgary_2010/IDTLogo.png"></img></a></td> | ||
Revision as of 19:06, 31 August 2010
Our modelling project consists of two components: a mathematical model done in MATLAB and an animation done in Autodesk Maya. We hope to model the formation of inclusion bodies, which are aggregations of misfolded protein that can occur within cells. You can click here to read more about our modelling project.
Description of Circuit 1 goes here.
Description of Circuit 2 goes here.
Description of Circuit 3 goes here. Lorem ipsum dolor sit amet, consectetur adipiscing elit. Sed commodo, nisl eget dictum scelerisque, magna arcu vulputate dolor, luctus elementum erat nulla nec ante. Etiam fermentum malesuada aliquet. In id augue tellus. Donec sollicitudin condimentum leo sit amet congue. Mauris ipsum ipsum, ultricies lobortis viverra vel, vestibulum quis turpis. Quisque ultrices faucibus nulla eget tristique. Nunc est lectus, dictum ac tempor at, pellentesque at erat. Nullam eu sollicitudin nisl. Integer rutrum, nulla eget semper pretium, sapien elit scelerisque lectus, eu vulputate eros nibh nec sapien. Duis convallis vehicula imperdiet. Cras suscipit sapien vel quam gravida porta.
Many synthetic biology projects involve the expression of recombinant proteins in microorganisms such as E. coli. The problems encountered with many synthetic biology projects often involve problems with protein expression. It is often very difficult to recognize the problem and pinpoint where it lies. The goal of the University of Calgary 2010 iGEM team is to build a protein expression "troubleshooting kit". This kit will contain two systems with which target genes can be inserted. In the resulting cell growth, fluorescent protein production will be used to determine whether there is a problem with protein expression as well as indicate where the protein expression is failing.
Protein expression happens in three steps: the transcription of the DNA to mRNA, the translation of mRNA into an amino acid sequence, and the folding of that amino acid sequence into a protein. Our system detects possible errors in these three steps using two circuits. The first circuit has a fluorescent reporter that is produced when DNA is transcribed into mRNA and another that is produced when mRNA is translated into a functional protein. When both reporter proteins are expressed in the cell, it indicates both transcription and translation are successful. The second circuit involves reporter systems that are activated as a result of protein misfolding. Two native stress-activated promoters from E. coli were engineered upstream to fluorescent reporters that will respond to periplasmic and cytoplasmic protein misfolding. If the protein of interest misfolds in either area of the cell, one of the promoters will be activated and the corresponding fluorescence will be observed.
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