Reporter
Part:BBa_K900000:Design
Designed by: Austin Jones Group: iGEM12_Berkeley (2012-09-27)
Design Notes
The gene was codon optimized for yeast and internal restriction sites were removed for compatibility with our Golden Gate cloning scheme.
Source
Synthesized in house and cloned into addgene plasmid [http://www.addgene.org/11911/ l11911] Previously engineered version of RFP from Subach et al., 2009.
References
Subach, F. V. et al. Photoactivatable mCherry for high-resolution two-color fluorescence microscopy. Nature Methods 6, 153–159 (2009).