Histonetters....We have received some dextran beads (coated with cells) that are "snap frozen"...for cutting.
We have done these beads before in histogel/paraffin...but are curious as to how best to handle them snap frozen. We have a nice bead with no cells on our first to snap frozen sample blocks....Help? Is it the temperature? We cut at -25 on average. _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
