Types | DnaRegion
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Roles | Coding
CDS
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Sequences | BBa_K562011_sequence (Version 1)
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Description
This is a composite part comprising a constitutive promoter, which is the tatABCD promoter from E. coli K-12, driving production of the initial 40 residues of the PduD protein from Salmonella enterica serovar Typhimurium LT2 (identical to part BBa_K562002), which is itself fused in-frame to mCherry. The mCherry gene product also carries a C-terminal HA epitope tag. Production of PduD40-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-D40-mCh in the Sargent Laboratory, Dundee, UK.
Notes
The natural pstI site within mCherry has been removed.
Source
Derived from Salmonella enterica serovar Typhimurium LT2 genomic sequence and an unknown cloning vector.