Find the right reagent for your research

DNA ladders / Mixed-increment DNA ladders / 50 bp to 10 kb fast-electrophoresis ladders / Ready-to-load ladders

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

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.

MGI library preparation

DNA library preparation kit specifically for the MGI sequencing platform; verify adapter and circularization requirements. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Illumina library preparation / Pre-fragmented double-stranded DNA libraries / Configuration requires review

Library preparation from already fragmented double-stranded DNA; use platform-compatible adapters and amplification primers. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

MGI library preparation

DNA library preparation kit specifically for the MGI sequencing platform; verify adapter and circularization requirements. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

MGI library preparation

DNA library preparation kit specifically for the MGI sequencing platform; verify adapter and circularization requirements. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Illumina library preparation / Pre-fragmented double-stranded DNA libraries / Configuration requires review

Library preparation from already fragmented double-stranded DNA; use platform-compatible adapters and amplification primers. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Bisulfite conversion / Purified DNA conversion / Spin-column cleanup

Bisulfite conversion of purified DNA followed by spin-column cleanup. 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.

One-step RT-qPCR / Probe RT-qPCR / Liquid mixes

Liquid probe-based one-step RT-qPCR reagents; supplied enzyme system and reference dye require protocol review. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.

Probe qPCR mixes / Liquid mixes

Liquid master mix for probe-based DNA qPCR. Check instrument reference-dye requirements and multiplex compatibility. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

N-glycan release / PNGase F / Rapid formulations

Rapid recombinant PNGase F without glycerol for N-glycan removal prior to chromatography or MS. The rapid buffer protocol must be matched; non-reducing suitability is not assumed.

Probe qPCR mixes / Liquid mixes

Liquid probe-based qPCR formulation; confirm instrument reference-dye requirements. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.

RT master mixes / RT mixes with gDNA removal

Reverse-transcription premix includes genomic DNA digestion reagents. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Dye qPCR mixes / Liquid mixes

Liquid intercalating-dye master mix for DNA qPCR; ROX and tracer-dye formulations differ. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.

Phosphatases / FastAP Thermosensitive Alkaline Phosphatase

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

AanI restriction enzymes / Fast-digest formulations

Restriction enzyme candidate from the manufacturer selection table. Verify recognition site, cleavage position, methylation sensitivity and buffer requirements. Name relationships do not establish identical behavior.

AasI restriction enzymes / Fast-digest formulations

Candidate only. Confirm substrate methylation, cleavage geometry, formulation and application suitability against current manufacturer documentation.

AatII restriction enzymes / Fast-digest formulations

Restriction enzyme candidate from the manufacturer selection table. Verify recognition site, cleavage position, methylation sensitivity and buffer requirements. Name relationships do not establish identical behavior.

Acc65I restriction enzymes / Fast-digest formulations

Restriction enzyme candidate from the manufacturer selection table. Verify recognition site, cleavage position, methylation sensitivity and buffer requirements. Name relationships do not establish identical behavior.

AdeI restriction enzymes / Fast-digest formulations

Restriction enzyme candidate from the manufacturer selection table. Verify recognition site, cleavage position, methylation sensitivity and buffer requirements. Name relationships do not establish identical behavior.

AjuI restriction enzymes / Fast-digest formulations

Restriction enzyme candidate from the manufacturer selection table. Verify recognition site, cleavage position, methylation sensitivity and buffer requirements. Name relationships do not establish identical behavior.

AluI restriction enzymes / Fast-digest formulations

Restriction enzyme candidate from the manufacturer selection table. Verify recognition site, cleavage position, methylation sensitivity and buffer requirements. Name relationships do not establish identical behavior.

Alw21I restriction enzymes / Fast-digest formulations

Restriction enzyme candidate from the manufacturer selection table. Verify recognition site, cleavage position, methylation sensitivity and buffer requirements. Name relationships do not establish identical behavior.