Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
Manufacturer catalog identifies the named restriction enzyme and catalog code. Isoschizomer aliases are not treated as interchangeable products; check cleavage position, methylation sensitivity, temperature and buffer. Confirm the supplier protocol, formulation and activity units before substitution.
Same enzyme identity candidate. Manufacturer page does not establish activity-unit equivalence, buffer compatibility, purity specification, or validated replacement for the existing product. Confirm these specifications before experimental substitution.
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
Cloned RNase I for sequence-independent RNA digestion. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RNase III cleaves double-stranded RNA substrates. 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.