Stand-alone enzyme with hot start mechanism for seamless integration into 1-step RT-qPCR reactions
Formulated for carry-over amplicon contamination control for use in automated, centralized pathogen testing workflows.
An inhibitor tolerant 2X master mix for endpoint or qPCR applications.
Selectively degrades inhibitory inorganic pyrophosphate in DNA synthesis reactions.
Versatile DNase used in NGS library preparation, Sanger sequencing, site-directed mutagenesis and nicked site extension applications.
Ideal for carryover amplicon prevention in qPCR, RT-qPCR, and RT-LAMP applications.
Removes DNA and RNA from viral particles (e.g. AAV), recombinant proteins, and other biomolecules under high salt conditions.
Expertly crafted enzymes, designed to streamline your processes and deliver consistent, high-quality results.