Team:Hong Kong-CUHK/project1.html

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                       <td class="subct" valign="top" style="background-color:#FFFFFF; padding:15px"><p style="margin-bottom: 10px" class="currentlink">Abstract</a></p>
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                         <p style="margin-bottom: 10px"  class="text"><a href="project2.html">Proj2</a></p>
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                   <td valign="top" style="background-color:#FFFFFF;padding:10px"><p class="aloveofthunder">Project1</p>
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                    <p>&nbsp;</p></td>
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<p>&nbsp;</p>
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<p class="aloveofthunder">Abstract</p>
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<p>Although the sensory technology has been deeply explored and implemented in various means, most of the developed sensors are chemically-dependent promoters which regulate downstream gene expression. We exploited the use of halobacterial sensors, the sensory rhodopsins which are sensitive to a wide spectrum of readily available light source and build a series of sensing systems to control cellular movement and gene regulation. This system can be executed as a fundamental part for further applications, such as cell targeting and refining. Furthermore, to counter the safety issues caused by the leakage of bioengineered cells, this sensing method altogether with the CRISPR/Cas sytem can targart and achieve the cleavage of the transformed plasmid under the stimulation of natural light sources.</p>
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Latest revision as of 14:22, 10 September 2012



 

 

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Project

Proj2

Proj3

 

 

Abstract

Although the sensory technology has been deeply explored and implemented in various means, most of the developed sensors are chemically-dependent promoters which regulate downstream gene expression. We exploited the use of halobacterial sensors, the sensory rhodopsins which are sensitive to a wide spectrum of readily available light source and build a series of sensing systems to control cellular movement and gene regulation. This system can be executed as a fundamental part for further applications, such as cell targeting and refining. Furthermore, to counter the safety issues caused by the leakage of bioengineered cells, this sensing method altogether with the CRISPR/Cas sytem can targart and achieve the cleavage of the transformed plasmid under the stimulation of natural light sources.

 


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