PME-mCherry no stop
 Construction details
pME-mCherry no stop was made by PCR amplification of mCherry, using primers that add att sites, followed by a BP reaction. Sequencing confirms that all bases of the insert are correct.
This clone can be used to generate N-terminal mCherry fusions with a gene of interest placed in a 3' clone.
Annotated sequence, Genbank format:
pME-mCherry no stop Genbank
FASTA file with the full-length sequence as well as sequences of individual components:
pME-mCherry no stop sequence