"
Team:Illinois/Protocols
From 2009.igem.org
m |
(→Standard) |
||
| (57 intermediate revisions not shown) | |||
| Line 1: | Line 1: | ||
{{UIUC09Temp}} | {{UIUC09Temp}} | ||
{{Illinois}} | {{Illinois}} | ||
| + | {{IllExpNav}} | ||
| - | == Protocols == | + | __NOTOC__ |
| + | |||
| + | <html> | ||
| + | <div id="uicontentbox"> | ||
| + | </html> | ||
| + | == '''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. | ||
| + | <html> | ||
| + | </div> | ||
| + | </html> | ||
| + | |||
| + | <html> | ||
| + | <div id="uicontentbox"> | ||
| + | </html> | ||
| + | |||
| + | == '''Standard''' == | ||
| + | *[http://www.biochem.northwestern.edu/morimoto/research/Protocols/I.%20Prokaryotes/A.%20Bacteriology.pdf Bacterial Culture Basics (media/plate preparation, growth, streaking, and storage)] | ||
| + | |||
| + | *[[Preparing Cryo stocks]] | ||
| + | |||
| + | *[http://www.stanford.edu/~teruel1/Protocols/pdf/Transformation%20Protocol%20Using%20Heat%20Shock.pdf Transformation by Heat Shock Protocol] | ||
| + | |||
| + | *[http://www.methodbook.net/dna/agarogel.html Agarose Gel Electrophoresis Protocol] | ||
| + | |||
| + | *[http://www.sigmaaldrich.com/life-science/custom-oligos/custom-dna/learning-center/annealing-oligos.html Annealing Oligonucleotides Protocol] | ||
| + | |||
| + | *[http://www1.qiagen.com/Products/DnaCleanup/GelPcrSiCleanupSystems/QIAquickPCRPurificationKit.aspx?r=1745#Tabs=t2 PCR Cleanup Protocol (QIAquick PCR Purification Kit)] -- Click on "QIAquick Spin Handbook - English (PDF)" under the "Handbooks" header | ||
| + | |||
| + | *[http://www.5prime.com/media/29661/perfectprep%20spin%20mini%20kit%20manual_5prime_1048299_072007.pdf Miniprep Protocol (PerfectPrep Spin Mini Kit)] | ||
| + | |||
| + | *[http://www.promega.com/tbs/tb374/tb374.pdf Miniprep Protocol (PureYield Plasmid Miniprep System)] | ||
| + | |||
| + | *[[BioBrick information]] | ||
| + | <html> | ||
| + | </div> | ||
| + | </html> | ||
| + | |||
| + | <html> | ||
| + | <div id="uicontentbox"> | ||
| + | </html> | ||
| + | |||
| + | == '''sRNA Characterization''' == | ||
| + | |||
| + | '''Taken from:''' [http://www.springerlink.com.proxy2.library.uiuc.edu/content/h752r3415261357p/ 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]]''' | ||
| + | <html> | ||
| + | </div> | ||
| + | </html> | ||
| + | |||
| + | <html> | ||
| + | <div id="uicontentbox"> | ||
| + | </html> | ||
| + | == '''Recipes''' == | ||
| + | |||
| + | [[LB Broth]] | ||
| + | |||
| + | [[LB Plates]] | ||
| + | |||
| + | [[EDTA]] | ||
| + | |||
| + | [[TAE Buffer]] | ||
| + | |||
| + | [[TBE Buffer]] | ||
| + | |||
| + | [[Agarose Gels]] | ||
| + | <html> | ||
| + | </div> | ||
| + | </html> | ||
| + | |||
| + | {{IllinoisBottomNav}} | ||
Latest revision as of 15:50, 10 August 2009
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.
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.stanford.edu/~teruel1/Protocols/pdf/Transformation%20Protocol%20Using%20Heat%20Shock.pdf Transformation by Heat Shock Protocol]
- [http://www.methodbook.net/dna/agarogel.html Agarose Gel Electrophoresis Protocol]
- [http://www.sigmaaldrich.com/life-science/custom-oligos/custom-dna/learning-center/annealing-oligos.html Annealing Oligonucleotides Protocol]
- [http://www1.qiagen.com/Products/DnaCleanup/GelPcrSiCleanupSystems/QIAquickPCRPurificationKit.aspx?r=1745#Tabs=t2 PCR Cleanup Protocol (QIAquick PCR Purification Kit)] -- Click on "QIAquick Spin Handbook - English (PDF)" under the "Handbooks" header
- [http://www.5prime.com/media/29661/perfectprep%20spin%20mini%20kit%20manual_5prime_1048299_072007.pdf Miniprep Protocol (PerfectPrep Spin Mini Kit)]
- [http://www.promega.com/tbs/tb374/tb374.pdf Miniprep Protocol (PureYield Plasmid Miniprep System)]
sRNA Characterization
Taken from: [http://www.springerlink.com.proxy2.library.uiuc.edu/content/h752r3415261357p/ 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.
Questions about our Wiki page? Please email us at illinoisiGEM@gmail.com.
