I am interested in obtaining a yeast vector with the following features:
CUP1 promoter-cloning sites-transcription terminator (such as PGK
terminator)-CEN/or 2 micron- HIS3 selectable marker.
Can someone point me to the information of comparing the promoter strength
of 1) constitutive promoter, such as GPD or ADH1 promoters; 2) GAL1-10
promoter; 3) CUP1 promoter? Thanks in advance for helps.
Department of Molecular Genetics
The Ohio State University
484 W. 12th Ave.
Columbus, OH 43210
chang.108 at osu.edu