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Team:BostonU/MoClo
From 2012.igem.org
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| - | <p style="text-align:center;"><a href="https://2012.igem.org/Team:BostonU"><img src=" | + | <p style="text-align:center;"><a href="https://2012.igem.org/Team:BostonU"><img src="https://static.igem.org/mediawiki/2012/6/64/Achievements.png" width="800px"></a></p> |
<ul id="nav"> | <ul id="nav"> | ||
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<ul> | <ul> | ||
<li><a href="https://2012.igem.org/Team:BostonU/Project_Overview">Project Overview and Abstract</a></li> | <li><a href="https://2012.igem.org/Team:BostonU/Project_Overview">Project Overview and Abstract</a></li> | ||
| - | <li><a href="https://2012.igem.org/Team:BostonU/Characterization">Introduction to Characterization</a></li> | + | <li><a href="https://2012.igem.org/Team:BostonU/MoClo2">Introduction to MoClo</a></li> |
| + | <li><a href="https://2012.igem.org/Team:BostonU/Characterization">Introduction to Characterization</a></li> | ||
| + | <li><a href="https://2012.igem.org/Team:BostonU/DataSheet">Introduction to Data Sheets</a></li> | ||
<li><a href="https://2012.igem.org/Team:BostonU/Methodology ">Methodology Overview</a></li> | <li><a href="https://2012.igem.org/Team:BostonU/Methodology ">Methodology Overview</a></li> | ||
| - | <li><a href="https://2012.igem.org/Team:BostonU/Results ">Results Summary</a></li> | + | <li><a href="https://2012.igem.org/Team:BostonU/Results ">Results Summary</a></li> |
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</li> | </li> | ||
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<li><a href="#">Considerations</a> | <li><a href="#">Considerations</a> | ||
<ul> | <ul> | ||
| - | <li><a href="https://2012.igem.org/Team:BostonU/ | + | <li><a href="https://2012.igem.org/Team:BostonU/NEGEM">New England iGEM Regional Meeting</a></li> |
<li><a href="https://2012.igem.org/Team:BostonU/Human Practices">Human Practices</a></li> | <li><a href="https://2012.igem.org/Team:BostonU/Human Practices">Human Practices</a></li> | ||
<li><a href="https://2012.igem.org/Team:BostonU/Safety">Safety</a></li> | <li><a href="https://2012.igem.org/Team:BostonU/Safety">Safety</a></li> | ||
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<h4>MoClo Kit</h4> | <h4>MoClo Kit</h4> | ||
<br> | <br> | ||
| - | < | + | <p> |
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| + | <img src="https://static.igem.org/mediawiki/2012/2/29/MoClokit.png" width="450"> | ||
| + | </p> | ||
| + | </center> | ||
| + | <ul> | ||
| + | <h7><p dir="ltr">One of our major contributions to the iGEM community is the submission of a MoClo Kit to the Registry. This kit is the summation of our MoClo Level 0 parts and Destination Vectors. For Level 0 parts, we currently have 17 promoters, 5 ribosomal bindiing sites, 3 genes, and 1 terminator. We are still working on expanding that list and will have updated numbers at the Jamboree. | ||
| + | <br><br> | ||
| + | At the time of the Wiki Freeze, our submitted parts included: | ||
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| + | <p> | ||
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| + | <img src="https://static.igem.org/mediawiki/2012/c/cb/Moclokitlist.png" width="700"> | ||
| + | <br><br><br> | ||
| + | <img src="https://static.igem.org/mediawiki/2012/8/89/Bumoclokit.png" width="600"> | ||
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| + | <p/></center> | ||
| + | <h7><p dir="ltr"> | ||
| + | <br><br> | ||
| + | We plan to add more parts to our Kit after the competition in order to complete our Kit so future iGEM teams can benefit from our efforts. These include all Level 2 Destination Vectors and some other parts that we failed to amplify this summer due to particularly troublesome PCRs (including repressible and inducible promoters and more genes). | ||
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| + | </html> | ||
Latest revision as of 03:15, 27 October 2012
MoClo Kit
One of our major contributions to the iGEM community is the submission of a MoClo Kit to the Registry. This kit is the summation of our MoClo Level 0 parts and Destination Vectors. For Level 0 parts, we currently have 17 promoters, 5 ribosomal bindiing sites, 3 genes, and 1 terminator. We are still working on expanding that list and will have updated numbers at the Jamboree.
At the time of the Wiki Freeze, our submitted parts included:
We plan to add more parts to our Kit after the competition in order to complete our Kit so future iGEM teams can benefit from our efforts. These include all Level 2 Destination Vectors and some other parts that we failed to amplify this summer due to particularly troublesome PCRs (including repressible and inducible promoters and more genes).
