Team:BostonU/MoClo

From 2012.igem.org

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<h7><p dir="ltr">With this number of Level 0 Parts, users can generate 255 number of unique Level 1 Parts. They will also be able to generate 45 unique 2-part Level 2 Parts, 28 unique 3-part Level 2 parts, and 13 unique 4-part Level 2 parts. The Level 2 Destination Vectors are in the process of being completed and will be submitted to the Registry upon confirmation but they will be submitted after the Wiki Freeze.
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We plan to add more parts to our Kit after the freeze, despite knowing that those parts will not be included in the judging for the competition. 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). We hope to have some of those parts finished by the Regional Jamboree.
We plan to add more parts to our Kit after the freeze, despite knowing that those parts will not be included in the judging for the competition. 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). We hope to have some of those parts finished by the Regional Jamboree.
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Revision as of 03:09, 27 October 2012

BostonU iGEM Team: Welcome


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 freeze, despite knowing that those parts will not be included in the judging for the competition. 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). We hope to have some of those parts finished by the Regional Jamboree.



    Bumoclokit.png