Difference between revisions of "Part:BBa J34100:Design"

(References)
(References)
Line 15: Line 15:
 
===References===
 
===References===
  
Simon L. Dove and Ann Hochschild, Conversion of the v subunit of ''Escherichia coli'' RNA polymerase into a transcriptional activator or an activation target, ''GENES & DEVELOPMENT'' 12:745–754
+
Simon L. Dove and Ann Hochschild, Conversion of the v subunit of ''Escherichia coli'' RNA polymerase into a transcriptional activator or an activation target, ''Genes and development'' 12:745–754
  
 
James C. Hu, Michael G. Kornacker, and Ann Hochschild, ''Escherichia coli'' One- and Two-Hybrid Systems
 
James C. Hu, Michael G. Kornacker, and Ann Hochschild, ''Escherichia coli'' One- and Two-Hybrid Systems
for the Analysis and IdentiÞcation of ProteinÐProtein Interactions, ''METHODS'' 20, 80Ð94 (2000)
+
for the Analysis and Identification of Protein Protein Interactions, ''Methods'' 20, 80Ð94 (2000)

Revision as of 15:03, 20 October 2006


AND gate, 2x PoPS input, 1x PoPS output


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 15
    Illegal EcoRI site found at 2963
    Illegal XbaI site found at 27
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 15
    Illegal EcoRI site found at 2963
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 15
    Illegal EcoRI site found at 2963
    Illegal BamHI site found at 9
    Illegal XhoI site found at 3048
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 15
    Illegal EcoRI site found at 2963
    Illegal XbaI site found at 27
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 15
    Illegal EcoRI site found at 2963
    Illegal XbaI site found at 27
    Illegal NgoMIV site found at 1968
    Illegal NgoMIV site found at 2087
    Illegal NgoMIV site found at 2702
    Illegal NgoMIV site found at 2711
    Illegal AgeI site found at 2262
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The initial promoters are omitted, so that the light sensing system can accept PoPs from another device, and the promoter on the end produces PoPs from this device

Source

When both the mRNA for the t7RNA polymerase and the tRNA that deactivates the early stop transcription are present, a functional t7RNA can be produced.

References

Simon L. Dove and Ann Hochschild, Conversion of the v subunit of Escherichia coli RNA polymerase into a transcriptional activator or an activation target, Genes and development 12:745–754

James C. Hu, Michael G. Kornacker, and Ann Hochschild, Escherichia coli One- and Two-Hybrid Systems for the Analysis and Identification of Protein Protein Interactions, Methods 20, 80Ð94 (2000)