Coding
PduD20-mCh

Part:BBa_K562010

Designed by: Frank Sargent   Group: iGEM11_Dundee   (2011-09-17)


Salty_PduD20-mCherry

This is a composite part comprising a constitutive promoter, which is the tatABCD promoter from E. coli K-12, driving production of the initial 20 residues of the PduD protein from Salmonella enterica serovar Typhimurium LT2 (identical to part BBa_K562001), which is itself fused in-frame to mCherry. The mCherry gene product also carries a C-terminal HA epitope tag. Production of PduD20-mCherry has been verified by Western immunoblotting (anti-mCherry). The construct is cloned as an EcoRI / PstI fragment into pSB1C3. The clone is also known as pSB-D20-mCh in the Sargent Laboratory, Dundee, UK.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 179
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 920
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 179
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 179
  • 1000
    COMPATIBLE WITH RFC[1000]


[edit]
Categories
Parameters
None