I'm cleaning so reusable probes that I use for RNA homogenization. I have looked at a few online guides about incubating the probes with 1% DEPC water but I am confused about the steps.
I incubated my probes wih 70% ethanol first and now I am incubating the probes in 1% DEPC water. For the DEPC step I just added the DEPC to water and submerged my probes in it. I'll incubate them over the weekend and then autoclave the probes that are submerged in DEPC water with a Liq20 cycle.
Is there anything wrong with those steps?
Edited by Wek, 08 August 2013 - 10:31 AM.