Difference between revisions of "Part:BBa K2623013:Experience"

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We do Enzyme-Cut identification to certify the plasmid is correct. We use the EcoR I and Pst I to cut the plasmid, which is the pSB1C3 containg the DNA sequence of BBa K2623013.(Fig.1)<br>
 
We do Enzyme-Cut identification to certify the plasmid is correct. We use the EcoR I and Pst I to cut the plasmid, which is the pSB1C3 containg the DNA sequence of BBa K2623013.(Fig.1)<br>
 
[[Image:K2623013.png|thumb|200px|Fig.1]]
 
[[Image:K2623013.png|thumb|200px|Fig.1]]
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Revision as of 05:07, 17 October 2018

Applications of BBa_K2623013

Identification

We do Enzyme-Cut identification to certify the plasmid is correct. We use the EcoR I and Pst I to cut the plasmid, which is the pSB1C3 containg the DNA sequence of BBa K2623013.(Fig.1)

Fig.1





























In order to verify the effectiveness of our Kai system, we verified the Escherichia coli that was transferred into the Kai loop under the fluorescence microscope after synchronization.
Since the Kai system is designed for periodic output of signals in Escherichia coli, we will evaluate the changes of fluorescent signals over time.

Fig.3 The bioluminescence at different times in GroupA. The negative value is cause by the value of the control group.
Fig.4 The bioluminescence at different times in GroupB. The negative value is cause by the value of the control group.

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