Hi,
We are trying to fractionate gut samples into RNA/DNA/protein using the
protocols in the Trizol handbook. The procedure works OK but we are having
difficulty resuspending the protein pellet at the end of the process 1% SDS
or 1M Tris pH10.4 has not done the trick. We are about to try the urea/CHAPS
protocol. Does anyone have any other ideas on how to bring the pellet back
into solution?
TIA
Ian Mc