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Template:Team:HokkaidoU Japan/Project/LeftContent
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* [[Team:HokkaidoU_Japan/Project/T3SS|Function of T3SS]] | * [[Team:HokkaidoU_Japan/Project/T3SS|Function of T3SS]] | ||
:: Detailed information about T3SS and summary of our achievements on iGEM 2010 | :: Detailed information about T3SS and summary of our achievements on iGEM 2010 | ||
| - | * [[Team:HokkaidoU_Japan/Project/Backbone|Ready-to-inject | + | * [[Team:HokkaidoU_Japan/Project/Onion|Injection assay using onion cells]] |
| + | :: Experiments using plant cells does not require much skills than using mammalian cultured cells | ||
| + | * [[Team:HokkaidoU_Japan/Project/Backbone|Ready-to-inject backbone and Bsa I cloning site]] | ||
:: Ready-to-inject backbone and Bsa I cloning site enable us to fuse T3S signal and protein easily | :: Ready-to-inject backbone and Bsa I cloning site enable us to fuse T3S signal and protein easily | ||
* [[Team:HokkaidoU_Japan/Project/GSK|GSK tag system]] | * [[Team:HokkaidoU_Japan/Project/GSK|GSK tag system]] | ||
| - | :: | + | :: A neat injection assay using GSK tag system, which can detect injected proteins specifically |
</div> | </div> | ||
Revision as of 20:46, 5 October 2011
- Detailed information about T3SS and summary of our achievements on iGEM 2010
- Experiments using plant cells does not require much skills than using mammalian cultured cells
- Ready-to-inject backbone and Bsa I cloning site enable us to fuse T3S signal and protein easily
- A neat injection assay using GSK tag system, which can detect injected proteins specifically
