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.
Human, mouse and rat rRNA depletion kit uses RNase H digestion; the listed components exclude purification beads. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
RNA library preparation / Selectable stranded and non-stranded RNA libraries / Illumina and MGI-compatible workflows
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.
Master mix for amplification during sequencing-library construction. Check whether platform-specific primers are included. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
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.
Exact named-enzyme comparison candidate. Use the supplier-specific buffer, incubation temperature, activity units and inactivation protocol. Review methylation sensitivity and star activity before substitution; this is not a validated drop-in replacement.
Affinity beads & resins / Immobilized metal affinity resins
Nickel-NTA agarose for immobilized-metal affinity purification of His-tagged proteins. Match capacity and imidazole, detergent and reducing-agent tolerances.
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
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.
Official product page specifies the named restriction enzyme and catalog number. Classified as a standard formulation; verify recognition sequence, methylation sensitivity, temperature and recommended buffer. Confirm formulation, activity units and experimental conditions before substitution.