Team:UC Chile/Cyanolux/Project short

From 2012.igem.org

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As there weren´t straighforward tools to start working with in the registry (i.e characterized plasmids backbones, protocols, etc) we started from scratch.
As there weren´t straighforward tools to start working with in the registry (i.e characterized plasmids backbones, protocols, etc) we started from scratch.
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We designed two recombination plasmids backbones.  One targets a gene essential for our chassis survival in the environment [https://2012.igem.org/Team:UC_Chile/Biosafety#Susceptibility_Construct
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We designed two recombination plasmids backbones.  One targets a gene essential for our chassis survival in the environment [https://2012.igem.org/Team:UC_Chile/Biosafety#Susceptibility_Construct (see biosafety)] and the other one a neutral site.
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see biosafety] and the other one a neutral site.
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[https://2012.igem.org/Team:UC_Chile/Cyanolux/Biolamp Full description of the device here]
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[https://2012.igem.org/Team:UC_Chile/Cyanolux/Biolamp Full description of the biolamp device here]
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[https://2012.igem.org/Team:UC_Chile/Cyanolux/Project See more about the whole project]
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<a href="https://2012.igem.org/Team:UC_Chile/Cyanolux/Results_short"><img src="https://static.igem.org/mediawiki/2012/a/ab/UC_Chile-Continue_button.jpg" align="right">
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<div style="float:right">
 
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[https://2012.igem.org/Team:UC_Chile/Cyanolux/Project See more about the project]
 
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Latest revision as of 03:23, 27 October 2012

Project: Luxilla - Pontificia Universidad Católica de Chile, iGEM 2012