RESEARCH. COMPARE. REVIEW.
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RNase inhibitors
Ribonuclease inhibitor for RNA workflows; concentration, formulation and manufacturing grade are product-specific. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RNase inhibitors
Ribonuclease inhibitor for RNA workflows; concentration, formulation and manufacturing grade are product-specific. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
MwoI restriction enzymes / Standard formulations
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
One-step RT-PCR / One-step RT-PCR kits
Candidate for the stated function. Confirm substrate, formulation, reaction conditions and application before substitution.
Glycan modification enzymes / Hexosaminidases
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Glycan modification enzymes / Glucosaminidases
Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. Removes terminal beta-linked N-acetylglucosamine.
Glycan binding proteins
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Modified nucleotides / N1-Methyl-Pseudouridine-5’-Triphosphate
100 mM N1-methylpseudouridine triphosphate sodium solution for modified RNA synthesis. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Modified nucleotides / N1-Methyl-Pseudouridine-5’-Triphosphate
100 mM N1-methylpseudouridine triphosphate Tris formulation for modified RNA synthesis. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Modified nucleotides / N1-Methyl-Pseudouridine-5’-Triphosphate
N1-methylpseudouridine triphosphate supplied as a 200 mM Tris solution for RNA synthesis; adjust concentration for the chosen reaction. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Modified nucleotides / N1-Methyl-Pseudouridine-5’-Triphosphate
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Modified nucleotides / N1-Methyl-Pseudouridine-5’-Triphosphate
N1-methylpseudouridine triphosphate sodium salt solution, 100-110 mM. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Modified nucleotides / N1-Methyl-Pseudouridine-5’-Triphosphate
Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. N1-methylpseudouridine triphosphate for RNA synthesis.
RNA capping / Cap analogs / m7G(5′)ppp(5′)A dinucleotide cap analogs
Dinucleotide m7GpppA cap analog; CAS 62828-63-1. Review cap orientation and transcript initiation requirements. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
NaeI 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.
NaeI 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.
NaeI restriction enzymes / Standard formulations
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
NarI 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.
NarI restriction enzymes / Standard formulations
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
N-glycan release / PNGase A
Native almond glycopeptidase A for N-glycan release from glycopeptides. Compare native substrate accessibility and required proteolytic pretreatment with recombinant PNGase A protocols.
Nb.BbvCI restriction enzymes / Standard formulations
Candidate only. Confirm substrate methylation, cleavage geometry, formulation and application suitability against current manufacturer documentation.
Nb.BbvCI restriction enzymes / Standard formulations
Candidate only. Confirm substrate methylation, cleavage geometry, formulation and application suitability against current manufacturer documentation.
Nb.BbvCI restriction enzymes / Standard formulations
Candidate only. Confirm substrate methylation, cleavage geometry, formulation and application suitability against current manufacturer documentation.
Nb.BbvCI restriction enzymes / Standard formulations
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
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