Team:University College London/Module 5/Characterisation

From 2012.igem.org

(Difference between revisions)
(Characterisation)
(Characterisation)
Line 9: Line 9:
IrrE is deduced to globally regulate gene expression in ''E. coli'', and to date, no specific assay allows for the convenient determination of IrrE expression. As such, the expression of IrrE will be determined indirectly by determining the increased salt tolerance of our cells. In order to confirm this, we will be conducting growth curve experiments. This will allow us to determine if our cell grow to a higher density in high salinity when compared to the untransformed cells.  
IrrE is deduced to globally regulate gene expression in ''E. coli'', and to date, no specific assay allows for the convenient determination of IrrE expression. As such, the expression of IrrE will be determined indirectly by determining the increased salt tolerance of our cells. In order to confirm this, we will be conducting growth curve experiments. This will allow us to determine if our cell grow to a higher density in high salinity when compared to the untransformed cells.  
-
As we will be using Lyon 2010 iGEM team's K540000 salt tolerance BioBrick for comparison, we will also attempt to replicate their results via growth rate experiments.  
+
As we will be using Lyon 2010 iGEM team's BBa_K540000 salt tolerance BioBrick for comparison, we will also attempt to replicate their results via growth rate experiments.  
{{:Team:University_College_London/templates/foot}}
{{:Team:University_College_London/templates/foot}}

Revision as of 14:46, 21 September 2012

Module 5: Salt Tolerance

Description | Design | Construction | Characterisation | Modelling | Results | Conclusions

Characterisation

IrrE is deduced to globally regulate gene expression in E. coli, and to date, no specific assay allows for the convenient determination of IrrE expression. As such, the expression of IrrE will be determined indirectly by determining the increased salt tolerance of our cells. In order to confirm this, we will be conducting growth curve experiments. This will allow us to determine if our cell grow to a higher density in high salinity when compared to the untransformed cells.

As we will be using Lyon 2010 iGEM team's BBa_K540000 salt tolerance BioBrick for comparison, we will also attempt to replicate their results via growth rate experiments.