Until now, I could not find a typical buffer, which I can use to dilute my antibodies and at the same time, keep spleen RNA from degrading? When I do the experiment, I cut the frozen spleen (- 20°C) and then I fix them by Ethanol 75%. After incubating the sample with Ab - short time- and doing the RNA extraction, I do not see RNA, even I do the experiment under ice conditions. Any suggestions?