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.
Thermostable RNase H for cleavage of RNA in RNA-DNA hybrids at elevated temperature. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Proofreading DNA polymerase or polymerase blend for high-fidelity PCR. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Manufacturer supplies water for molecular biology tested free of DNase and RNase; verify the current ordering size. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Molecular biology water is tested for absence of DNase and RNase activity. Candidate for this workflow; follow the supplier protocol and validate input and instrument compatibility.
Two-step kit provides reverse transcription followed by a separate endpoint PCR amplification workflow. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
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.
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.
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.
Methylation controls / Human or mouse genomic DNA / Unconverted
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.
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.
RNA library construction reagents can follow separate mRNA enrichment or rRNA depletion. Upstream RNA selection is not supplied as an interchangeable selection module. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RNA library construction reagents can follow separate mRNA enrichment or rRNA depletion. Upstream RNA selection is not supplied as an interchangeable selection module. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
DNA templates / Lambda DNA (N6-methyladenine-free)
Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. Lambda DNA free of bacterial dam/dcm methylation; verify required site methylation status.
UPstart Plus monoclonal Taq-inhibiting antibody at 1 mg/ml; validate the antibody-to-enzyme ratio for hot-start PCR. Review the manufacturer protocol before substituting.
Monoclonal Taq-inhibiting antibody at 1 mg/ml for constructing antibody-mediated hot-start PCR; titrate against the selected polymerase. Review the manufacturer protocol before substituting.