A wide range of applications

Host-cell DNA contamination confounds results and reduces quality. Salt-active nucleases remove it at lysis, improving consistency and data reliability.

Efficient host-DNA depletion with salt-active nucleases turns metagenomics into a same-day, pan-pathogen diagnostic tool—see how.

Our nucleases are, especially salt tolerant and tailor made for viral bioprocessing, which results in a less expensive and more efficient process.

To prevent PCR carry-over, the PCR mixture is treated with uracil DNA glycosylase (UNG).

IsoPol™BST⁺ is well suited for isothermal applications such as LAMP and RT-LAMP for its superior amplification performance and robustness.

Cod UNG is the ideal contamination control in RT-LAMP as it effectively eliminates false positive results from carry-over contaminants and restores assay sensitivity.

With our Heat&Run gDNA removal kit the removal of contaminating genomic DNA from RNA is easier than ever before.

Our PCR Decontamination kit removes contaminating DNA in master mixes without reduction of PCR sensitivity.

SAP offers a simple and effective method for removing nucleotides and primers from PCR products prior to sequencing or genotyping.

SAP completely dephosphorylates the DNA in a single, and simple incubation. There is no need for complex calculations and multi-step incubations.

HL-SAN is easily inactivated by treatment with a reducing agent, and the high pI (9.6) enables easy separation of HL-SAN from most protein targets.

SAN is perfectly suitable for the complete removal of DNA.

SAN is the perfect enzyme to reduce the viscosity in BugBuster lysates.