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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 | + | *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. |
*6/18--Restriction and purification of genes and target sequences were successful. | *6/18--Restriction and purification of genes and target sequences were successful. | ||
*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. | *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. | ||
Revision as of 15:30, 18 June 2009
Home
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!
For a description of our project idea, please see our Project page. Please also view our [http://openwetware.org/wiki/IllinoisSyntheticBio OpenWetWare page] to see early project development.
Our team works very closely with the Illinois Tools team. Please visit their Wiki page to view their project.
Announcements
- 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.
- 6/18--Restriction and purification of genes and target sequences were successful.
- 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.
- 6/17--A Strain List page has been created under the Project heading that will list the strains of bacteria we have created in lab.
- 6/16--Please view our Notebook page to view our lab progress.
- 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.
- 6/11--The Notebook page is now set up. Lab group pages will be set up as research begins.
- 6/9--The Research page is now set up.
- 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.
- 6/7--The Team page is now set up.
- 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.
- 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.
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!
Questions about our Wiki page? Please email Dave Korenchan at korench1@illinois.edu.
