Candidate category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.
Clarify whether RNA has already undergone phase separation; not every crude phenol lysate is accepted. Direct crude phenol-lysate handling not established.
Spin-column RNA cleanup after extraction; manufacturer specifies up to 50 µg RNA and 20-50 µL elution. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Candidate category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.
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.
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.
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.
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.
Loading dyes / RNA loading buffers / Formamide denaturing buffers / Bromophenol blue and xylene cyanol with ethidium bromide
Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. Loading reagent for RNA gels, not protein loading buffer.
Combinatorial dual-index primer set with separate i5 and i7 combinations for Illumina RNA libraries; not a unique-dual-index set. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Combinatorial dual-index primer set with separate i5 and i7 combinations for Illumina RNA libraries; not a unique-dual-index set. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
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.
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.
Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. Nine single-stranded RNA transcripts from 281 to 6583 bases.
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.
Kit combines E. coli poly(A) polymerase, ATP and reaction reagents for RNA 3-prime polyadenylation. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
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.
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.
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.
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.
General sample nucleic acid extraction / Spin-column purification
Sequential resin spin-column DNA, RNA and protein purification from cells, tissues, blood and microbes. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.