Difference between revisions of "Part:BBa J69511"

 
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<partinfo>BBa_J69511 short</partinfo>
 
<partinfo>BBa_J69511 short</partinfo>
  
Hi, we are from NTU-Singapore and we have made single basepair mutants of the RBS used in this reporter construct.
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Hi, we are from NTU-Singapore and we have made single basepair mutants of the RBS used in this reporter construct, BBa_B0034
  
1AT denotes substitution of A to T.
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1AT denotes substitution of A to T at the first base pair position, so on so forth. Based on BBa_B0034, we mutated all 12 base pairs of the RBS by changing each base with the other three bases. These mutants were then characterise in Shewanella oneidensis MR1.
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Our library entry can be found from BBa_K1676037 to BBa_K1676072 where GFP expression monitoring data can be found. :)
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https://static.igem.org/mediawiki/2015/4/49/MUTATIONS.png
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Results of the mutant library:
  
 
https://static.igem.org/mediawiki/2015/3/3a/Rbs-spots.jpeg
 
https://static.igem.org/mediawiki/2015/3/3a/Rbs-spots.jpeg
  
Our library entry can be found from BBa_K1676037 to BBa_K1676072.
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https://static.igem.org/mediawiki/2015/9/90/Sumary.png
  
  

Latest revision as of 04:58, 20 September 2015

GFP reporter device - LacI repressible

Hi, we are from NTU-Singapore and we have made single basepair mutants of the RBS used in this reporter construct, BBa_B0034

1AT denotes substitution of A to T at the first base pair position, so on so forth. Based on BBa_B0034, we mutated all 12 base pairs of the RBS by changing each base with the other three bases. These mutants were then characterise in Shewanella oneidensis MR1.

Our library entry can be found from BBa_K1676037 to BBa_K1676072 where GFP expression monitoring data can be found. :)

MUTATIONS.png

Results of the mutant library:

Rbs-spots.jpeg

Sumary.png


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 725