Difference between revisions of "Part:BBa K4164018"
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<p style="text-align: center!important;"><b>Figure1.YFP fluorescence intensity after 30 mins incubation under different temperatures. </b></p>
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<p style="text-align: center!important;"><b>Figure2. Effect of different IPTG concentrations on YFP expression</b></p>
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<p style="text-align: center!important;"><b>Figure3. 4 hours YFP-transformed E. coli strains (Right: control) </b></p>
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<b>Figure3. 4 hours YFP-transformed E. coli strains (Right: control) </b></p>
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here
 
===Usage and Biology===
 
===Usage and Biology===

Revision as of 12:06, 11 October 2022


Contribution

This composite part is used to do further research on the yellow fluorescent protein (YFP), which is commonly used as the reporter of a gene circuit. We chose the Bobrick BBa_K592101 from the iGEM distribution kit and recombined it to plasmid pET-29a+ by homologous recombination. We firstly studied the effect of different concentration of IPTG(Isopropyl-beta-D-thiogalactopyranoside) on the expression of YFP and the fluorescence intensity of bacteria. After that, we also extracted the YFP from the bacteria and identified the effect of temperature on YFP activity.

Figure1.YFP fluorescence intensity after 30 mins incubation under different temperatures.

Figure2. Effect of different IPTG concentrations on YFP expression

Figure3. 4 hours YFP-transformed E. coli strains (Right: control)

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 741