Difference between revisions of "Part:BBa K902008:Design"
 
Line 9: Line 9:
  
 
===Source===
 
===Source===
−
The <i>E.coli genome</i>. Synthesized through IDT
+
The <i>E.coli</i> genome. Synthesized through IDT
  
 
===References===
 
===References===
 
1) Cromie MJ, Groisman EA. Promoter and riboswitch control of the Mg2+ transporter MgtA from Salmonella enterica. J Bacteriol 2010 Jan;192(2):604-607.
 
1) Cromie MJ, Groisman EA. Promoter and riboswitch control of the Mg2+ transporter MgtA from Salmonella enterica. J Bacteriol 2010 Jan;192(2):604-607.

Latest revision as of 03:08, 4 October 2012

MgtA riboswitch


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
    COMPATIBLE WITH RFC[1000]


Design Notes

There are no illegal cut sites in this brick and any changes to the DNA can result in inactivation through changes in the secondary structure of the RNA motif.

Source

The E.coli genome. Synthesized through IDT

References

1) Cromie MJ, Groisman EA. Promoter and riboswitch control of the Mg2+ transporter MgtA from Salmonella enterica. J Bacteriol 2010 Jan;192(2):604-607.