Team:Illinois

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== Home ==
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Welcome to the home page of the Illinois iGEM 2009 Wet Lab team!  This is our second year in the iGEM (International Genetically Engineered Machine) competition, so we are very excited. We have been working very hard, and we are sure that our project will be very successful!
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The Illinois iGEM team has been working to engineer a decoder function within E. coli. Decoders are logic devices used frequently in low-level computer architecture. We are creating a 2 to 4 decoder, which takes two binary inputs to activate one of four outputs. Each output corresponds to a specific combination of the inputs. With the presence of lactose and arabinose, our Bacterial Decoder will express Green Fluorescent Protein. If only lactose is present, a different fluorescent protein will be expressed. This goes for the other two combinations as well (only arabinose, or neither sugars). To implement logic we use combinations of small non-coding RNAs and transcription factors. The system allows the next engineer to swap standard parts in and out to change the inputs and outputs. Our Bacterial Decoder can help sense for multiple environmental cues, having implications for medical diagnostics and environmental and water contaminant detection.
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For a description of our project idea, please see our [https://2009.igem.org/Team:Illinois/Project Project page].  Please also view our [http://openwetware.org/wiki/IllinoisSyntheticBio OpenWetWare page] to see early project development.
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For a more detailed description of our project, please see our [https://2009.igem.org/Team:Illinois/Project Project page].
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Our team is also excited about the project that the [https://2009.igem.org/Team:Illinois-Tools Illinois Tools team] has chosen.  Please visit their Wiki page to view their project.
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Our team works very closely with the [https://2009.igem.org/Team:Illinois-Tools Illinois Tools team].  Please visit their Wiki page to view their project.
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== '''Announcements''' ==
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*7/14--Our Wiki is undergoing construction.  Hopefully a new side navigation bar will be successfully added.
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*7/13--Added some pretty hilarious [https://2009.igem.org/Team:Illinois/Team#Fun_Things videos] to the team page. Work in the lab is progressing, but ligations are still proving difficult.
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*6/30--We have reorganized lab groups again.  The sRNA Library and Modeling groups will remain the same.  The other two groups have become two new groups: the Hybrid Promoter group and the 3'-Acting sRNAs group.
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*6/27--Check out our new iGEM video on the Home page!
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*6/26--Meagan is leaving for Spain tomorrow to study abroad!  Bye, Meagan!  We'll all miss you!!!
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*6/24--Our team has split up into four groups working on four different aspects of the project: the sRNA library, mRNA degradation, sRNA dual regulation, and modeling.  As a result, the Notebook page has been reorganized.
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*6/19--Our Wiki page has just been reorganized.  There is now an Experiments tab that includes the Protocols, Plasmids, and Strain List pages.
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*6/18--We are experiencing difficulties in replicating our plasmid DNA.  In the past couple days, our gels have continually reported a DNA fragment that is smaller than the one we expected to see, and today our streak plates are missing.  We hope to rectify the situation as soon as possible so we may resume work.
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*6/18--Restriction and purification of genes and target sequences were successful.
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*6/17--All of the sRNA genes and target sequences have been successfully made by PCR and verified by gel electrophoresis.  We will be adding restriction endonucleases and purifying our genes and target sequences today.
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*6/17--A [https://2009.igem.org/Team:Illinois/Strain_List Strain List] page has been created under the Project heading that will list the strains of bacteria we have created in lab.
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*6/16--Please view our [https://2009.igem.org/Team:Illinois/Notebook Notebook] page to view our lab progress.
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*6/11--We expect to begin lab work on Monday!  Four groups will be working for the next week to characterize four different sRNAs via target sequence-GFP fusions and add them to the Parts Registry.
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*6/11--The Notebook page is now set up.  Lab group pages will be set up as research begins.
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*6/9--The Research page is now set up.
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*6/9--We have changed a lot on the Wiki page.  The Sponsors and Pictures sections, as well as the Protocols, Research, Modeling, and Parts pages, are under construction.  Announcements will be posted when each page/section is set up.
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*6/7--The Team page is now set up.
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*6/1--The Team, Protocols, Resources, Parts, Notebook, and Pictures pages are still under construction.  Please check back regularly, as announcements will be posted when these pages are set up.
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*6/1--We are currently ordering supplies, as we will begin lab work as soon as possible.  We are also continuing research on sRNAs and deciding on which model to use for our project.  Testing various parts in the lab will help influence our final decision for a model to use.
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== '''Sponsors''' ==
== '''Sponsors''' ==
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<a href="http://www.igb.uiuc.edu/"><img src="/wiki/images/0/04/Igbsponsor.png"></a>
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We are very grateful to our sponsors for allowing us to compete in the 2009 iGEM competition.  Thank you for all your contributions to the Illinois iGEM 2009 Team!
We are very grateful to our sponsors for allowing us to compete in the 2009 iGEM competition.  Thank you for all your contributions to the Illinois iGEM 2009 Team!
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== Donations ==
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If you would like to make a financial donation to the Illinois iGEM Team, you may do so online.  Please click on the link below.  Thank you!
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http://www-app.igb.uiuc.edu/igem/donate.php
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Latest revision as of 02:36, 22 October 2009

Click to go to the Illinois home page



Home
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Home

The Illinois iGEM team has been working to engineer a decoder function within E. coli. Decoders are logic devices used frequently in low-level computer architecture. We are creating a 2 to 4 decoder, which takes two binary inputs to activate one of four outputs. Each output corresponds to a specific combination of the inputs. With the presence of lactose and arabinose, our Bacterial Decoder will express Green Fluorescent Protein. If only lactose is present, a different fluorescent protein will be expressed. This goes for the other two combinations as well (only arabinose, or neither sugars). To implement logic we use combinations of small non-coding RNAs and transcription factors. The system allows the next engineer to swap standard parts in and out to change the inputs and outputs. Our Bacterial Decoder can help sense for multiple environmental cues, having implications for medical diagnostics and environmental and water contaminant detection.

For a more detailed description of our project, please see our Project page.

Our team is also excited about the project that the Illinois Tools team has chosen. Please visit their Wiki page to view their project.

Sponsors

 

We are very grateful to our sponsors for allowing us to compete in the 2009 iGEM competition. Thank you for all your contributions to the Illinois iGEM 2009 Team!

Donations

If you would like to make a financial donation to the Illinois iGEM Team, you may do so online. Please click on the link below. Thank you!

http://www-app.igb.uiuc.edu/igem/donate.php

Questions about our Wiki page? Please email us at illinoisiGEM@gmail.com.

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