Difference between revisions of "Part:BBa K1807001:Design"

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===Design Notes===
 
===Design Notes===
  
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This part was sub-cloned from the pBC9 plasmid, first described by Akiyama et al., 1993.
+
This part was sub-cloned from the pBC9 plasmid, first described by Akiyama et al., 1993. iGEM York 2015 obtained pBC9 with Dr Jay Keasling's assistance.
  
 
The primer pair used to PCR clone the part:
 
The primer pair used to PCR clone the part:

Revision as of 23:29, 18 September 2015

Escherichia coli Exopolyphosphatase (PPX)


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 SapI.rc site found at 872


Design Notes

This part was sub-cloned from the pBC9 plasmid, first described by Akiyama et al., 1993. iGEM York 2015 obtained pBC9 with Dr Jay Keasling's assistance.

The primer pair used to PCR clone the part:

Forward: AGCACATACGAGAAAGAGGAGAAATACcccATGCCAATACACGATAAATCCCCT

Reverse: GAGCCTTTCGTTTTATTTGATGCCTGGcccTTAAGCGGCGATTTCTGGTGTACT


Source

Escherichia coli BW25113

References