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Indexes & adapters / Library primers
Library amplification primer mix for Illumina library preparation; RNA versus DNA adapter structures require confirmation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
PCR cleanup / Magnetic bead purification
SPRI magnetic DNA cleanup beads recover fragments from 50 bp to 20 kb and remove primers, nucleotides, salts and proteins. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
DNA size selection / Magnetic bead purification
SPRI magnetic beads for DNA size selection in NGS workflows; manufactured in an ultra-clean facility. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
RNA library preparation / Selectable stranded and non-stranded RNA libraries / Illumina and MGI-compatible workflows
RNA library preparation reagents compatible with separately prepared mRNA or rRNA-depleted input; strand specificity depends on formulation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
T4 DNA ligases / Liquid enzymes
Verify substrate, formulation, activity units, buffers and experimental conditions before substitution.
Strand-displacing polymerases / Engineered Bst DNA polymerases
Engineered Bst-family strand-displacing DNA polymerase; concentration and liquid or lyophilized formulation require protocol review. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Nanopore library preparation
Nanopore DNA library preparation reagent kit; compatible barcodes and sequencing adapters require separate confirmation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RNA extraction / Magnetic bead purification
Magnetic-bead total RNA extraction from animal and plant tissues and cells; supports automated platforms. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Magnetic capture beads / Silica-coated magnetic beads
Silica-coated superparamagnetic particles with silicon hydroxyl surface groups for nucleic acid binding; standalone beads require a compatible buffer system. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Strand-displacing polymerases / Engineered Bst DNA polymerases
Engineered Bst-family strand-displacing DNA polymerase; concentration and liquid or lyophilized formulation require protocol review. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Strand-displacing polymerases / Engineered Bst DNA polymerases
Engineered Bst-family strand-displacing DNA polymerase; concentration and liquid or lyophilized formulation require protocol review. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
T7 transcription / RNA polymerase enzymes
T7 RNA polymerase for promoter-directed RNA synthesis; concentration and production grade differ. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
T7 transcription / RNA polymerase enzymes
T7 RNA polymerase for promoter-directed RNA synthesis; concentration and production grade differ. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
T7 transcription / RNA polymerase enzymes
T7 RNA polymerase for promoter-directed RNA synthesis; concentration and production grade differ. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Strand-displacing polymerases / Warm-start Bst DNA polymerases / Standard formulations
Warm-start Bst DNA polymerase for strand-displacement amplification with temperature-dependent activation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RT master mixes / RT mixes with gDNA removal
See datasheet. HiExact-series reverse transcription mix with gDNA removal.
RT master mixes / RT mixes with gDNA removal
See datasheet. Second-generation first-strand supermix package with a genomic-DNA digestion step.
RT master mixes / RT mixes with gDNA removal
Mixed primers. 4× Hifair III RT formulation with random primers and oligo(dT)18.
Guide RNA synthesis
Verify substrate, formulation, activity units, buffers and experimental conditions before substitution.
First-strand cDNA synthesis kits
First-strand cDNA synthesis kit with a dye-free formulation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RT master mixes / RT mixes with gDNA removal
First-strand cDNA synthesis premix includes genomic DNA digestion. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Reverse transcriptase enzymes / Engineered reverse transcriptases
Engineered reverse transcriptase for cDNA synthesis; glycerol content and concentration vary by formulation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Reverse transcriptase enzymes / Engineered reverse transcriptases
Engineered reverse transcriptase for cDNA synthesis; glycerol content and concentration vary by formulation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Reverse transcriptase enzymes / Engineered reverse transcriptases
Engineered reverse transcriptase for cDNA synthesis; glycerol content and concentration vary by formulation. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
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