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Team:Bielefeld-Germany/Protocols2
From 2012.igem.org
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<img src="https://static.igem.org/mediawiki/2011/9/9a/Bielefeld-Germany2011-Thermocycler-klein.jpg"/> | <img src="https://static.igem.org/mediawiki/2011/9/9a/Bielefeld-Germany2011-Thermocycler-klein.jpg"/> | ||
<strong>Immobilization</strong> | <strong>Immobilization</strong> | ||
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<img src="https://static.igem.org/mediawiki/2011/6/6c/Bielefeld-Germany2011-analyticsklein.JPG" /> | <img src="https://static.igem.org/mediawiki/2011/6/6c/Bielefeld-Germany2011-analyticsklein.JPG" /> | ||
<strong>Material</strong> | <strong>Material</strong> | ||
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| - | Genetic engineering is a basic tool of synthetic biology. With the help of standardized DNA building blocks (BioBricks) it is fairly easy to create new and modify existing natural systems. The methods we have used in our project to create BioBricks and to modify, mutate, transform and analyse DNA are presented in this section. Methods used: Electroporation; chemical transformation; Standard, Freiburg, Gibson and 3A BioBrick assembly; restriction analysis; colony PCR; site directed mutagenesis. <a href="https:// | + | Genetic engineering is a basic tool of synthetic biology. With the help of standardized DNA building blocks (BioBricks) it is fairly easy to create new and modify existing natural systems. The methods we have used in our project to create BioBricks and to modify, mutate, transform and analyse DNA are presented in this section. Methods used: Electroporation; chemical transformation; Standard, Freiburg, Gibson and 3A BioBrick assembly; restriction analysis; colony PCR; site directed mutagenesis. <a href="https://2012.igem.org/Team:Bielefeld-Germany/Protocols/molecular_genetics">read more</a> |
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<img src="https://static.igem.org/mediawiki/2012/c/c1/Bielefeld2012_Production_300.jpg" /> | <img src="https://static.igem.org/mediawiki/2012/c/c1/Bielefeld2012_Production_300.jpg" /> | ||
| - | <h3><a style="text-decoration:none; color:black;" href="https:// | + | <h3><a style="text-decoration:none; color:black;" href="https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Production">Production</a></h3> |
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| - | Before one is able to work with a cell-free system based on biological material, the needed proteins have to be produced and purified first. These methods and the ones we used to characterize BioBricks in vivo are presented in this section. Used methods: Cultivations in shaking flasks and bioreactor; protein clean-up from medium, periplasm, whole cell and inclusion bodies; UF / DF; IEX; Ni-NTA columns and chromatography; recrystallization and immobilization of S-layer proteins. <a href="https:// | + | Before one is able to work with a cell-free system based on biological material, the needed proteins have to be produced and purified first. These methods and the ones we used to characterize BioBricks in vivo are presented in this section. Used methods: Cultivations in shaking flasks and bioreactor; protein clean-up from medium, periplasm, whole cell and inclusion bodies; UF / DF; IEX; Ni-NTA columns and chromatography; recrystallization and immobilization of S-layer proteins. <a href="https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Production">read more</a> |
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<img src="https://static.igem.org/mediawiki/2012/6/60/Bielefeld2012_Activity_300.jpg" /> | <img src="https://static.igem.org/mediawiki/2012/6/60/Bielefeld2012_Activity_300.jpg" /> | ||
| - | <h3><a style="text-decoration:none; color:black;" href="https:// | + | <h3><a style="text-decoration:none; color:black;" href="https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Analytics">Analytics</a></h3> |
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| - | DNA and proteins are very small and cannot be seen by the naked eye. To control the success and the results of your upstream and downstream processes, analytical methods are necessary that give reliable results to make DNA or proteins in any way visible for you. The analytical methods we used in our project can be found in this section. Used methods: Fluorescence measurement; SDS-PAGE; MALDI-TOF; HPLC; LC-ESI-qTOF-MS/MS; molecular beacons; extraction. <a href="https:// | + | DNA and proteins are very small and cannot be seen by the naked eye. To control the success and the results of your upstream and downstream processes, analytical methods are necessary that give reliable results to make DNA or proteins in any way visible for you. The analytical methods we used in our project can be found in this section. Used methods: Fluorescence measurement; SDS-PAGE; MALDI-TOF; HPLC; LC-ESI-qTOF-MS/MS; molecular beacons; extraction. <a href="https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Analytics">read more</a> |
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| + | <img src="https://static.igem.org/mediawiki/2011/2/26/Bielefeld-Germany2011-MaterialMethods300px.JPG" /> | ||
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| + | <h3><a style="text-decoration:none; color:black;" href="https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Imobilization">Immobilization</a></h3> | ||
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| + | <p class="more"> | ||
| + | Here you can find out, how we immobilized the produced enzymes. | ||
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| + | <p> | ||
| + | Coming soon <a href="https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Immobilization">read more</a> | ||
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| + | </div> | ||
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<img src="https://static.igem.org/mediawiki/2011/2/26/Bielefeld-Germany2011-MaterialMethods300px.JPG" /> | <img src="https://static.igem.org/mediawiki/2011/2/26/Bielefeld-Germany2011-MaterialMethods300px.JPG" /> | ||
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| - | Chemical and biological reactions need defined conditions to work as expected. The chemicals, enzymes, kits, buffers and media we used in our project are listed in this section. <a href="https:// | + | Chemical and biological reactions need defined conditions to work as expected. The chemicals, enzymes, kits, buffers and media we used in our project are listed in this section. <a href="https://2012.igem.org/Team:Bielefeld-Germany/Protocols/Materials">read more</a> |
</p> | </p> | ||
Revision as of 09:00, 13 September 2012
Molecular
Genetic engineering protocols
Production
Upstreaming and downstreaming
Analytics
Analytical methods
Material
Enzymes, kits, chemicals, buffers
Molecular
In this section of our protocol pages you can read more about our methods for cloning and BioBrick assembly.
Genetic engineering is a basic tool of synthetic biology. With the help of standardized DNA building blocks (BioBricks) it is fairly easy to create new and modify existing natural systems. The methods we have used in our project to create BioBricks and to modify, mutate, transform and analyse DNA are presented in this section. Methods used: Electroporation; chemical transformation; Standard, Freiburg, Gibson and 3A BioBrick assembly; restriction analysis; colony PCR; site directed mutagenesis. read more
Production
These are the protocols for the cultivations and the downstream processing.
Before one is able to work with a cell-free system based on biological material, the needed proteins have to be produced and purified first. These methods and the ones we used to characterize BioBricks in vivo are presented in this section. Used methods: Cultivations in shaking flasks and bioreactor; protein clean-up from medium, periplasm, whole cell and inclusion bodies; UF / DF; IEX; Ni-NTA columns and chromatography; recrystallization and immobilization of S-layer proteins. read more
Analytics
Protocols for the analytical methods we used.
DNA and proteins are very small and cannot be seen by the naked eye. To control the success and the results of your upstream and downstream processes, analytical methods are necessary that give reliable results to make DNA or proteins in any way visible for you. The analytical methods we used in our project can be found in this section. Used methods: Fluorescence measurement; SDS-PAGE; MALDI-TOF; HPLC; LC-ESI-qTOF-MS/MS; molecular beacons; extraction. read more
Immobilization
Here you can find out, how we immobilized the produced enzymes.
Coming soon read more
