Difference between revisions of "Part:BBa K1132038:Design"

 
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===Source===
 
===Source===
  
−
synthesis
+
Cloning assembly.
  
 
===References===
 
===References===
 +
[http://www.ncbi.nlm.nih.gov/pubmed/23539178 ''Amplifying genetic logic gates.'' Bonnet et al.]<br>
 +
[http://www.ncbi.nlm.nih.gov/pubmed/23396014 ''Synthetic circuits integrating logic and memory in living cells.'' Siuti et al.]

Latest revision as of 03:24, 5 October 2013


XOR-inverted RFP gate (BBa_K1132035) with T7 polymerase under the control of a strong promoter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1116
    Illegal NheI site found at 1139
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 178
    Illegal AgeI site found at 290
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

This BioBrick is design to test the XOR gate (BBa_K1132004) by measuring the level of RFP after recombination events. The biobrick Bba_K081014 containing the RBS site, the coding sequence of the RFP and a terminator have been inserted inside our gate between the FimE restrictions sites. The T7 polymerase gene is also present in the biobrick, under the control of a strong promoter, strong RBS. This part can therefore be used stand-alone as all elements to control the RFP output are present.


Source

Cloning assembly.

References

[http://www.ncbi.nlm.nih.gov/pubmed/23539178 Amplifying genetic logic gates. Bonnet et al.]
[http://www.ncbi.nlm.nih.gov/pubmed/23396014 Synthetic circuits integrating logic and memory in living cells. Siuti et al.]