Candidate category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.
Candidate category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.
Proofreading OptiTaq master mix containing two gel-tracking dyes for direct loading. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Hot-start Taq enzyme; activation mechanism and protocol must match the selected formulation. Color products include tracking dyes. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Antibody-mediated hot-start Taq master mix with two gel-tracking dyes. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Proofreading enzyme or enzyme blend for high-fidelity PCR; activation, end structure and cycling conditions vary by formulation. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Taq DNA polymerase for routine endpoint PCR; the Color formulation contains tracking dyes. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Standard PCR / Master mixes / Ready-to-load PCR mixes
Routine Taq PCR master mix with two gel-tracking dyes. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Single-index adapters for Illumina DNA library preparation; each adapter carries one sample index. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Single-index adapters for Illumina DNA library preparation; each adapter carries one sample index. 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.
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.
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 category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.
DNA modification enzymes / SssI (CpG) Methyltransferase
Candidate category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.