Team:Freiburg/Project

From 2011.igem.org

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By eliminating routine use of expensive materials, this novel assay will utilize sustainable laboratory equipment and widespread His-Tag technology.
By eliminating routine use of expensive materials, this novel assay will utilize sustainable laboratory equipment and widespread His-Tag technology.
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We propose an expression system induced by blue, green and red light, combined with subsequent temperature controlled autolysis of E. coli.  
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We propose an expression system induced by blue, green and red light, combined with subsequent temperature controlled autolysis of ''E. coli''.  
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Purification of the protein of interest will be accomplished by  
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Purification of the his-tagged protein of interest will be accomplished by  
an adaptor protein of our own design which binds the His-Tag on one side and the surface of serological pipettes on the other. Two subsequent pipetting steps for washing and purification of the cell lysate will quickly elute the product.
an adaptor protein of our own design which binds the His-Tag on one side and the surface of serological pipettes on the other. Two subsequent pipetting steps for washing and purification of the cell lysate will quickly elute the product.
Our system will provide expression and purification of Polymerase and Ligase, but will be easily expandable to any His-Tagged protein needed by the modern molecular biologist.
Our system will provide expression and purification of Polymerase and Ligase, but will be easily expandable to any His-Tagged protein needed by the modern molecular biologist.
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Revision as of 13:18, 14 July 2011


This is the wiki page
of the Freiburger student
team competing for iGEM 2011.
Thank you for your interest!