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Standard PCR / Standalone enzymes
Standalone non-proofreading Taq DNA polymerase for endpoint amplification. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Standard PCR / Standalone enzymes
Standalone Taq DNA polymerase for endpoint PCR. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Standard PCR / Standalone enzymes
Taq DNA polymerase for routine endpoint PCR; the Color formulation contains tracking dyes. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Standard PCR / Standalone enzymes
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Standard PCR / Standalone enzymes
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Standard PCR / Standalone enzymes
Recombinant Taq at 5 U/µl for routine endpoint PCR; not a proofreading enzyme. Review the manufacturer protocol before substituting.
Standard PCR / Kits
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Standard PCR / Master mixes / PCR mixes without specified loading dye
Routine Taq PCR master mix with buffer, magnesium and dNTPs; no loading dye specified. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Long-range PCR / Standalone enzymes
Taq and proofreading-polymerase blend specified for amplification of long DNA templates. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Standard PCR / Standalone enzymes
Standalone Taq-family endpoint PCR enzyme; check the presence or absence of 5-prime exonuclease activity. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Standard PCR / Standalone enzymes
N-terminally truncated Taq polymerase for non-proofreading endpoint PCR. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
TaqI restriction enzymes / Standard formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
TaqI restriction enzymes / Standard formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
TaqI restriction enzymes / Standard formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
TaqI restriction enzymes / Standard formulations
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.
DNA modification enzymes / TaqI Methyltransferase
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
DNA modification enzymes / TaqI Methyltransferase
Candidate for the stated function. Confirm substrate, formulation, reaction conditions and application before substitution.
TaqI restriction enzymes / Fast-digest formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
TaqI restriction enzymes / Standard formulations
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Probe qPCR mixes / Liquid mixes
Catalog category candidate. Experimental interchangeability has not been validated.
One-step RT-qPCR / Probe RT-qPCR / Formulation unspecified
Catalog category candidate. Experimental interchangeability has not been validated.
Primer-free RT mixes
Reverse transcription reaction mix is supplied without embedded primers; separate oligo(dT) and random primers allow user-selected priming. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Protelomerases / TelA protelomerase
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Protelomerases / TelN protelomerase
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
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