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Team:Edinburgh/Project/Future
From 2010.igem.org
(Difference between revisions)
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<ul> | <ul> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Project/Protocol">the protocol</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Project/Protocol">the protocol</a></li> | ||
| - | <li><a href="https://2010.igem.org/Team:Edinburgh | + | <li><a href="https://2010.igem.org/Team:Edinburgh/BioBricks#Genomic">submitted parts</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Results#Genomic">results</a></li> |
<li><a href="https://2010.igem.org/Team:Edinburgh/Project/Future">future work</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Project/Future">future work</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Project/References">references</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Project/References">references</a></li> | ||
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<li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Green_light_producer">green light</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Green_light_producer">green light</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Green_light_sensor">green sensor</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Green_light_sensor">green sensor</a></li> | ||
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial | + | <li><a href="https://2010.igem.org/Team:Edinburgh/BioBricks#Bacterial">submitted parts</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Results#Bacterial">results</a></li> |
<li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Future">future work</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/Future">future work</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/References">references</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Bacterial/References">references</a></li> | ||
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<li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Bacterial">the bacterial model</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Bacterial">the bacterial model</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Signalling">the signalling model</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Signalling">the signalling model</a></li> | ||
| - | <li><a href="https://2010.igem.org/Team:Edinburgh | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Results#Modelling">results</a></li> |
<li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Future">future work</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/Future">future work</a></li> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/References">references</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Modelling/References">references</a></li> | ||
| Line 83: | Line 83: | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Human" class="dir">human BRIDGEs</a> | <li><a href="https://2010.igem.org/Team:Edinburgh/Human" class="dir">human BRIDGEs</a> | ||
<ul> | <ul> | ||
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Human">human aspects</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/Aspects">human aspects</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Human">results</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/Epic">the epic</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Human">future work</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Results#Human">results</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Human">references</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/Future">future work</a></li> |
| + | <li><a href="https://2010.igem.org/Team:Edinburgh/Human/References">references</a></li> | ||
</ul> | </ul> | ||
</li> | </li> | ||
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<ul> | <ul> | ||
<li><a href="https://2010.igem.org/Team:Edinburgh/Notebook">collaboration</a></li> | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook">collaboration</a></li> | ||
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook">BRIDGE</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/BRIDGE">BRIDGE</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook">red light</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Red_light_producer">red light</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook">red sensor</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Red_light_sensor">red sensor</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook">blue light</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Blue_light_producer">blue light</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook">blue sensor</a></li> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Blue_light_sensor">blue sensor</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook"> | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Modelling">modelling</a></li> |
| - | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook | + | <li><a href="https://2010.igem.org/Team:Edinburgh/Notebook/Safety">safety</a></li> |
| - | + | ||
<li><a href="http://www.openwetware.org/wiki/French_Lab">protocols</a></li> | <li><a href="http://www.openwetware.org/wiki/French_Lab">protocols</a></li> | ||
</ul> | </ul> | ||
Revision as of 11:36, 3 September 2010
Sequential Addition
One of the future expansions of BRIDGE which we have discussed is using it to directly introduce genes in the genome next to each other without using the BioBrick method before-hand. If you wanted to insert 4 genes with the steps described in the protocol section, it would take 8 steps. If you do this with the method below it would take 4 steps.
At the first step of the process, the first antibiotic resistance gene and sacB are introduced alongside the first gene. The antibiotic resistance gene can then be replaced with the next gene and a second antibiotic resistance gene, thereby cycling the antibiotic resistance such that selection is different at each step. At the last step, both markers are removed and the final constructs can be selected for by growth on sucrose (growth on sucrose can also be used as a negative control at each stage, although this would only be to confirm the persistance of the marker).
The final construct would look as below:
This has not been tested, but the principle is not too distant from the original method, so it would be nice to demonstrate it if anyone ever gets the chance.
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