Team:DTU-Denmark-2

From 2011.igem.org

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Revision as of 17:40, 19 September 2011

Revolutionizing Synthetic Biology

We have designed a novel standardized assembly system, called “Plug 'n' Play with DNA” where ready to use biological parts can directly be gathered without the use of restriction enzymes and ligases. This will make synthetic biology faster and assembly of expression vectors possible within a few hours. We have created a library of standardized biological parts for mammalian cells and fungi ready to plug 'n' play. You can find more information about how this standard works here.

Creating a reporter system

As proof of concept we in very short time created a reporter system that could be used for anything from monitoring gene expression to determination of protein localization. We chose to express and/or localize fluorescent proteins in the model organism Aspergillus nidulans and the mammalian cell line U-2 OS with great success.

Flexibility

Standardization entails rigidity. We acknowledge this and have therefore written a guide that allows the user to customize the system. In this way proteins can be assembled seamless, multiple mutations can be introduced in one cloning round, the only thing setting a limit is your creativity.

Applications

Here you can learn more about the numerous applications of the Plug’n’Play with DNA assembly standard and the situations where the use of this system is especially advantageous.

Data Page

You can find an overview of our project on our Data Page. This is also the place where you can find our favorite submitted biobricks and all the biobricks we characterized during the summer.

Achievements

Designing a novel assembly standard and creating a reporter system for Aspergillus nidulans and mammalian cells are our main achievements. You can read more find more information on our accomplishments on this page.

The Team

We have been five girls working on this project two and a half month projects with support from our three supervisors. You can learn more about us and how we started an iGEM team on our Team Page.

iGEM 2011 Wiki Main Page

Sponsored by

Comments or questions to the team? Please Email us

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