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Team:LMU-Munich/Lab Notebook/Protocols
From 2012.igem.org
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6. [https://static.igem.org/mediawiki/2012/6/6d/LMU-Munich_2012_Clean_deletions_in_Bacillus_subtilis.pdf Clean deletion of genomic fragments in ''Bacillus subtilis''] | 6. [https://static.igem.org/mediawiki/2012/6/6d/LMU-Munich_2012_Clean_deletions_in_Bacillus_subtilis.pdf Clean deletion of genomic fragments in ''Bacillus subtilis''] | ||
| - | Protocol for the production of markerless gene deletions. You will need the [http://www.ncbi.nlm.nih.gov/pubmed/15528558 pMAD] plasmid. This method is more time consuming than inserting | + | Protocol for the production of markerless gene deletions. You will need the [http://www.ncbi.nlm.nih.gov/pubmed/15528558 pMAD] plasmid. This method is more time consuming than inserting resistance cassettes but offers better cell perfomance. |
Revision as of 15:16, 3 September 2012
The LMU-Munich team is exuberantly happy about the great success at the World Championship Jamboree in Boston. Our project Beadzillus finished 4th and won the prize for the "Best Wiki" (with Slovenia) and "Best New Application Project".
[ more news ]
Protocols
On this page, we will upload unique protocols to share with the public.
Since we work with Bacillus subtilis as chassis we focus on protocols how to work with that organism.
1. Media and components for Bacillus subtilis
This protocol gives the recipes for various media and the antibiotic concentrations used for B. subtilis.
2. Transformation of Bacillus subtilis
Protocol how to transform B. subtilis.
3. Isolation of chromosomal DNA from Bacillus subtilis for transformation
A quick protocol how to isolate genomic DNA from B.subtilis to transform it to a different strain. By this mean you can very easily combine different B. subtilis genotypes. transformation of genomic DNA is much more efficient than plasmids. Isolated DNA with this protocol is not clean!
4. Isolation of chromosomal DNA from Bacillus subtilis (for PCR....)
Isolation of pure genomic DNA from B. subtilis.
PCR protocol for long flanking homology PCR. You might need those PCR products for interrupting genes with resistance cassettes.
6. Clean deletion of genomic fragments in Bacillus subtilis
Protocol for the production of markerless gene deletions. You will need the [http://www.ncbi.nlm.nih.gov/pubmed/15528558 pMAD] plasmid. This method is more time consuming than inserting resistance cassettes but offers better cell perfomance.
Protocol to count efficiency of sporulation and germination.
8. ß-Galactosidase Assay B. subtilis
Protocol how to measure lacZ gene activity in B. subtilis
