RNase I hydrolyzes RNA with preference for single-stranded substrates and has no DNA nuclease activity. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
E. coli RNase III for double-stranded RNA processing. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Ribonuclease inhibitor for RNA-sensitive enzyme reactions. Confirm the inhibited RNase classes and reducing conditions. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Recombinant RNase inhibitor for protecting RNA in enzymatic workflows. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Recombinant RNase inhibitor for RNA-sensitive enzymatic reactions. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RNase R for processive digestion of linear RNA; structured substrates require protocol review. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
RNase R exonuclease for degradation of linear RNA; manufacturing grade differs. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RNase R exonuclease for degradation of linear RNA; manufacturing grade differs. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Ribonuclease inhibitor for RNA-sensitive enzyme reactions. Confirm the inhibited RNase classes and reducing conditions. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Tissue-specific input and phase separation requirements; not general all-sample extraction. Tissue-specific reagent system; general sample and arbitrary phenol-lysate compatibility are unverified.
RNA 5′ end processing / RNA 5′ pyrophosphohydrolase (RppH)
Bacterial RppH converts triphosphorylated RNA 5-prime ends to monophosphate ends. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Candidate category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.