Modified Taq polymerase activated by high-temperature incubation. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Hot-start PCR master mix with red tracking dye for direct gel loading. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Two-fold concentrated chemically modified hot-start Taq master mix; no loading dye is specified. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Standalone temperature-activated Taq-family PCR enzyme. Activation chemistry and extension conditions vary by product. Candidate for the listed workflow; compare buffer, sample input and protocol requirements 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. 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.
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.