yeast cDNA library strategy
storez at cochin.inserm.fr
Wed Feb 6 11:42:00 EST 2002
I am currently constructing a yeast cDNA library ( 3 Reading frame vector,
directed cloning SSTI/NotI, fusion protein-cDNA construct). I would like to
know the number of clones you need to obtain after bacterial
transformation (primary clones), before making the transformation of the
library in yeast.
For the ligation of cDNA into the vector, what are the important steps to do
for defining the optimal ratio of cDNA / vector ?
What is the strategy after transfection in Bacteria (plating/cDNA library
Thank you very much in advance,
storez at icgm.cochin.inserm.fr
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