Find the right reagent for your research

Deoxynucleotides / Nucleotide mixes & sets

Four separate 100 mM dATP, dCTP, dGTP and dTTP solutions. Review the manufacturer protocol before substituting.

Deoxynucleotides / Nucleotide mixes & sets

Manufacturer product page lists dNTP Set, 100 mM each with catalog number DN4400 for molecular biology reactions. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.

DpnI 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.

DpnI 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.

DpnI 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.

DpnI restriction enzymes / Standard formulations

Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.

DpnII restriction enzymes / Standard formulations

Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.

DpnII restriction enzymes / Standard formulations

Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.

DraI 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.

DraI 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.

DraI 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.

DraI 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.

DraI 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.

DraI restriction enzymes / Standard formulations

Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.

DraIII restriction enzymes / High-fidelity formulations

Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.

DrdI restriction enzymes / Standard formulations

Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.

Standard PCR / Standalone enzymes

Catalog category candidate. Experimental interchangeability has not been validated.

Genomic DNA extraction / Spin-column purification

Spin-column genomic DNA extraction from dried blood spots. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.

Genomic DNA extraction / Magnetic bead purification

Magnetic-bead DNA isolation from dried blood spots. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.

Genomic DNA extraction / Spin-column purification

Spin-column extraction of genomic DNA from dried blood spots and small blood, urine or saliva samples. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.

Translation additives / Disulfide bond enhancers

DsbC and oxidized glutathione supplement for disulfide-bond formation in PUREfrex cell-free protein synthesis. Validate compatibility with other reconstituted translation systems.

DNA fragmentation

Catalog category candidate. Experimental interchangeability has not been validated.

DNA fragmentation

Candidate category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.

Double-stranded DNA-specific nucleases

Compare thermal inactivation, substrate specificity and activity definitions.