pTurboGFP-B is a prokaryotic expression vector encoding green fluorescent protein TurboGFP (see reporter description). Reporter codon usage is optimized for high expression in mammalian cells (humanized) [Haas et al., 1996].

The vector is primarily intended as a source of TurboGFP coding sequence. Flanking restriction sites are convenient for excision of TurboGFP sequence and its further insertion into other expression vectors of choice. Alternatively, TurboGFP coding sequence can be amplified by PCR.

Note: The plasmid DNA was isolated from dam⁺-methylated E. coli. Therefore some restriction sites are blocked by methylation. If you wish to digest the vector using such sites you will need to transform the vector into a dam^- host and make fresh DNA.

The vector can be also used for TurboGFP expression in prokaryotes under the control of T5 promoter/lac operator. The vector backbone contains ColE1 origin of replication and ampicillin resistance gene for propagation and selection in E. coli.