*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy*****
Dear all,
we started to clone with mAmetrine and mTagBFP and we got some issue with
fusion constructs that would otherwise work with EGFP. Also, mTagBFP seems to
aggregate easily.
I am aware that this is quite a generic question, but I wished to ask around to
see if others had issue with these specific two fluorescent proteins.
Cheers,
Alessandro