Difference between revisions of "Part:BBa K389013:Design"

 
(Design Notes)
Line 1: Line 1:
 
 
__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K389013 short</partinfo>
 
<partinfo>BBa_K389013 short</partinfo>
Line 7: Line 6:
  
 
===Design Notes===
 
===Design Notes===
medium strong constitutive promotor, terminator to keep basal expression of mRFP low
+
* medium strong constitutive promoter
 
+
* double terminator (forward) to keep basal expression of mRFP low  
 
+
** double terminator <partinfo>BBa_B0017</partinfo> instead of <partinfo>BBa_B0015</partinfo> because of problems mentioned with <partinfo>BBa_B0012</partinfo>
 +
* mRFP gene to show the activity of the ''vir'' promoter
  
 
===Source===
 
===Source===

Revision as of 12:42, 7 October 2010

VirA reporter system mRFP


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
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1686
    Illegal AgeI site found at 1798
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

  • medium strong constitutive promoter
  • double terminator (forward) to keep basal expression of mRFP low
  • mRFP gene to show the activity of the vir promoter

Source

parts.igem, synthetic gene by Mr. Gene, TI-plasmid from Agrobacterium tumefaciens C58

References