Difference between revisions of "Part:BBa K1431812"
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===Usage and Biology===
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===Selective Figures===
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<center>https://static.igem.org/mediawiki/parts/a/a1/SUSTC-Shenzhen-Project-P41016-112140.jpg</center>
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<center>LB agar plate of Biobricks BBa_K1431812 after incubating 23h at 37℃
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<center>https://static.igem.org/mediawiki/parts/f/fc/SUSTC-Shenzhen-Project-P41017-024507.jpg</center>
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<center>LB broth of Biobricks BBa_K1431812 after incubating 11h at 37℃,180rpm
  
 
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Revision as of 00:45, 18 October 2014

amilCP, blue chromoprotein reporter system (Strong Promoter, Strong RBS)

Team Uppsala 2012 chromoprotein attracts many interests because its more convenient than fluorescent protein to be use as a reporter. However, few characterized data can be found for these proteins. SUSTC-Shenzhen this year want to tackle with theses problems.

We've constructed a series of plasmids which are all in the same pattern: a strong/weak promoter, a strong/weak RBS and a chromoprotein. We want to monitor the speed of expression of these plasmids in normal incubation conditions (like 37℃ overnight for LB agar plate and 37℃ 180rpm for LB broth). The expression speed and strength of the constructed biobricks will be carefully monitored and gave others a relative scale for using chromoprotein as a reporter gene.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]