Find the right reagent for your research

Proteases / Furin

Recombinant human furin produced in HEK293S cells. Match cleavage sequence, activity units and calcium requirements.

Sanger sequencing cleanup / Spin-column purification

G-50 gel-filtration spin columns remove unincorporated sequencing dye terminators; DNA fragments above 20 bases are recovered. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.

Wash buffers / Formulation compatibility unspecified

Requires review: exact composition, calibration, formulation, kit or hardware compatibility, or regulatory identity is not fully established by the captured manufacturer description. Shared function is insufficient for substitution.

Glycan modification enzymes / Galactosidases / beta 1-3,4 Galactosidase

Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. Beta-galactosidase mixture removes beta1-3,4 terminal galactose.

Glycan modification enzymes / Galactosaminidases

Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. Alpha-N-acetylgalactosaminidase for terminal GalNAc removal.

Structure-specific nucleases / NEBExpress GamS Nuclease Inhibitor

Verify substrate, formulation, activity units, buffers and experimental conditions before substitution.

Cloning E. coli / 10-beta strains

Chemically competent GB10B cells described by the manufacturer as DH10B-equivalent. Compare full genotype, DNA size and transformation efficiency.

Electrocompetent E. coli / 10-beta strains

Electrocompetent DH10B-equivalent cloning cells. Confirm electrical transformation protocol and efficiency for the intended construct.

Electrocompetent E. coli / 10-beta strains

High-efficiency electrocompetent DH10B-equivalent cells for demanding and large-construct cloning applications. Verify insert-size requirements.

Cloning E. coli / 5-alpha strains

Chemically competent GB5-alpha cells described by the manufacturer as DH5-alpha-equivalent. Verify genotype and efficiency for the intended cloning experiment.

DNA fragmentation

Enzyme system fragments double-stranded DNA for sequencing library construction. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

DNA end and damage repair / Combined end repair and dA-tailing modules

DNA end-preparation module combines end repair and dA-tailing for library preparation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Adapter ligation

DNA ligation module for attaching sequencing adapters; adapter chemistry and concentration must be matched. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Hot-start PCR / Standalone enzymes

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.

Reverse transcriptase enzymes / Engineered reverse transcriptases

Engineered M-MLV-derived reverse transcriptase with increased thermal stability; formulation and inhibitor tolerance require protocol review. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Hot-start PCR / Standalone enzymes

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.

Hot-start PCR / Standalone enzymes

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.

Reverse transcriptase enzymes / Engineered reverse transcriptases

Engineered M-MLV-derived reverse transcriptase with increased thermal stability; formulation and inhibitor tolerance require protocol review. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

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.

Illumina library preparation / Enzymatic fragmentation libraries

Illumina DNA library kit combines enzymatic fragmentation, end repair and dA-tailing before adapter ligation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Gel extraction / Spin-column purification

Glass-fiber spin-column agarose gel DNA extraction with pH-indicator binding buffer. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.

Loading dyes / DNA loading buffers / Bromophenol blue with SDS

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

Loading dyes / DNA loading buffers / Orange G with SDS

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

Loading dyes / DNA loading buffers / UV-transparent tracking dyes with SDS

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