Difference between revisions of "Part:BBa K2623011:Experience"
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| + | <br>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.<br> | ||
| + | Since the Kai system is designed for periodic output of signals in Escherichia coli, we evaluateD the changes of fluorescent signals over time. Here are the curves we made. More details can be found in http://2018.igem.org/Team:XMU-China/Measurement | ||
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| + | <table><tr><th> | ||
| + | [[Image:GroupA.png|thumb|400px|Fig.3 The bioluminescence at different times in GroupA. The negative value is cause by the value of the control group.]]</th><th> | ||
| + | [[Image:GroupB.png|thumb|400px|Fig.4 The bioluminescence at different times in GroupB. The negative value is cause by the value of the control group.]]</th><th></table> | ||
===User Reviews=== | ===User Reviews=== | ||
Revision as of 05:14, 17 October 2018
Applications of BBa_K2623011
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 K2623011.(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 evaluateD the changes of fluorescent signals over time. Here are the curves we made. More details can be found in http://2018.igem.org/Team:XMU-China/Measurement
User Reviews
UNIQdcfcacfe3b21eee7-partinfo-00000000-QINU UNIQdcfcacfe3b21eee7-partinfo-00000001-QINU