I am using QIAGEN's AllPrep DNA/RNA/miRNA Universal Kit. The handbook doesn’t mention the possibility of additional DNase digestion post-elution, i.e. directly in the RNA solution.
Can this additional in-solution DNase digestion (and/or subsequent DNase heat (65-75C) inactivation) damage miRNA or lower yield and so should one only use in-column DNase digestion as per protocol?