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Action of RNases A and V1 on the 2.8-kb D-HITs. Total RNA from induced Daudi/ATCC cells was treated with excess single (RNase A)- or double (RNase V1)-stranded RNA-specific RNases at 20°C for 30 min. Products were separated by electrophoresis and visualized after transfer to nitrocellulose and hybridization with a 32P-labelled EBV BamHI-Ia probe (A) or probes for rRNAs (B).
