I'm currently making some GAL4-cDNA fusion libraries for two-hybrid
screening. Does anyone know how to control the RT reaction so that it's
efficient enough to to give decent first strands, and yet not hit the 5'
UTR ? (that'll mess up the fusion junction with GAL4 on the vector)
Thanks a 10e6!
Institute of Molecular Agrobiology
National University of Singapore
PS. Any tips to make sure I get all 3 frames in the right 5'-3' orientation?