Team:BostonU/MoClo
From 2012.igem.org
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<h4>MoClo Kit</h4> | <h4>MoClo Kit</h4> | ||
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+ | <img src="https://static.igem.org/mediawiki/2012/2/29/MoClokit.png" width="450"> | ||
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- | <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. | + | <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. |
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At the time of the Wiki Freeze, our submitted parts included: | At the time of the Wiki Freeze, our submitted parts included: | ||
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+ | <img src="https://static.igem.org/mediawiki/2012/c/cb/Moclokitlist.png" width="700"> | ||
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+ | <img src="https://static.igem.org/mediawiki/2012/8/89/Bumoclokit.png" width="600"> | ||
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+ | 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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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).