Team:Illinois/Protocols

From 2009.igem.org

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== '''Protocols''' ==
== '''Protocols''' ==
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This page describes protocols or includes links to protocols used in our project.  Recipes used are also listed in a separate section.  Protocols are organized by category.
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This page describes protocols or includes links to protocols used in our project.  Recipes used are also listed in a separate section.  Protocols are organized by category.  They were collected from Open Wet Ware, our advisors, and labs around the University of Illinois campus.
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== '''Standard''' ==
== '''Standard''' ==
*[http://www.biochem.northwestern.edu/morimoto/research/Protocols/I.%20Prokaryotes/A.%20Bacteriology.pdf Bacterial Culture Basics (media/plate preparation, growth, streaking, and storage)]
*[http://www.biochem.northwestern.edu/morimoto/research/Protocols/I.%20Prokaryotes/A.%20Bacteriology.pdf Bacterial Culture Basics (media/plate preparation, growth, streaking, and storage)]

Revision as of 00:04, 18 July 2009

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Contents

Protocols

This page describes protocols or includes links to protocols used in our project. Recipes used are also listed in a separate section. Protocols are organized by category. They were collected from Open Wet Ware, our advisors, and labs around the University of Illinois campus.

sRNA Characterization

Taken from: A Green Fluorescent Protein (GFP)-Based Plasmid System to Study Post-Transcriptional Control of Gene Expression In Vivo: Johannes H. Urban and Jörg Vogel, 2009

This protocol is used to characterize an E. coli small RNA and its ability to downregulate a reporter gene (GFP). The small RNA is cloned out of the E. coli chromosome and inserted into a high-copy number plasmid (pJU-334). The sRNA's target sequence is also cloned out of the E. coli chromosome and inserted into a low-copy number plasmid (pXG-10). Both plasmids are then transformed into E. coli Top10F' cells. Successful sRNA repression is indicated by a decreased level of fluorescence in the cells.

sRNA characterization procedure

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