Team:Illinois/Protocols

From 2009.igem.org

(Difference between revisions)
Line 41: Line 41:
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.
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]]'''
<html>
<html>
</div>
</div>
</html>
</html>
-
'''[[sRNA characterization procedure]]'''
 
<html>
<html>

Revision as of 00:04, 18 July 2009

Click to go to the Illinois home page





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


Questions about our Wiki page? Please email us at illinoisiGEM@gmail.com.