Enzymes

Glycerol-free, high concentration enzyme used with in isothermal amplification method such as LAMP, RPA, RCA, SDA and tHDA)

Thermostable high fidelity Hot Start DNA polymerase, generates blunt-ended amplicons up to 5 kb in length making it ideal for high yields in NGS library amplification.

Very high yield, high-performance, antibody-mediated hot-start polymerase, to give fast, superior amplification, even with challenging templates and in the presence of PCR inhibitors.

Highly purified Taq DNA polymerase with low DNA background and stringent chemical hot-start properties, ideal for PCR of low-copy bacterial targets to avoid false-positive amplification, such as in water testing.

Lyophilization-compatible high-performance Taq DNA polymerase, separate Taq antibody and enzyme dilution buffer, suitable for difficult, multiplex tests that require fast amplification, whilst maintaining high specificity and sensitivity.

DNA polymerase (exo-), with strand-displacement properties. used for Isothermal DNA amplification such as LAMP (Loop-mediated Isothermal Amplification).

Glycerol-free, high concentration hot-start Taq DNA polymerase, suitable for difficult, multiplex molecular tests that require fast amplification.

High concentration glycerol-free DNA polymerase (exo-), with strand-displacement properties. used for Isothermal DNA amplification such as LAMP (Loop-mediated Isothermal Amplification).

Glycerol-free high concentration reverse transcriptase and dilution buffer. Can be used to create 1-step RT-qPCR mixes for subsequent lyophilization.

For the detection of RNA at very low levels, it can also be used with a broader temperature range, making it ideal for applications such as blood bank or transplant viral testing.

For cDNA synthesis and subsequent PCR or qPCR in a one-step or two-step assay.

Used to eliminate carryover polymerase chain reaction (PCR) products in qPCR and RT-qPCR,by incorporating dUTP in reactions, so residual products from previous PCR amplifications containing dUs can be digested.

Proteinase K Solution is an enzyme used to digest most proteins in molecular biological techniques.

Highly robust, thermostable reverse transcriptase, ideal for cDNA synthesis from RNA with a high secondary structure such as viral RNA genomes.

Glycerol-free, high concentration, high fidelity DNA polymerase with separate dilution and reaction buffer, ideal for NGS library amplification and gene expression. Ideal for lyophilization.

Glycerol-free, high concentration enzyme that efficiently joins blunt and cohesive ends and repairs single stranded nicks in duplex DNA, RNA or DNA/RNA hybrids. Ideal for lyophilization.

Glycerol-free, high concentration DNA-dependant RNA Polymerase that requires a T7 promoter sequence, it an ideal enzyme for in-vitro synthesis of labeled or unlabeled RNA for research, diagnostic or clinical applications. Ideal for lyophilization.

Glycerol-free, high concentration RNA-specific endonuclease that hydrolyzes the phosphodiester bonds of RNA, when hybridized to DNA. Ideal for lyophilization.

Glycerol-free, high concentration, high fidelity DNA polymerase with separate dilution and reaction buffer, ideal for NGS library amplification and gene expression. Ideal for lyophilization.

Glycerol-free, high concentration, thermostable DNA polymerase with intrinsic reverse transcriptase (RT) activity and unlike other RT enzymes, it is not associated with RNase H activity. Ideal for lyophilization.

Glycerol-free enzyme used to phosphorylate the ends of both DNA and RNA during labeling and ligation, mainly used in next-generation sequencing (NGS) library preparation. Ideal for lyophilization.

Glycerol-free, high concentration DNA polymerase used for generating blunt ends on any duplex DNA molecule, used in next-generation sequencing (NGS) library preparation. Ideal for lyophilization.

Glycerol-free, high concentration DNA polymerase used for generating blunt ends on any duplex DNA molecule, used in next-generation sequencing (NGS) library preparation. Ideal for lyophilization.

Glycerol-free, high concentration DNA Pol I Klenow Fragment exo-, designed for dA- and dT-tailing for next-generation sequencing (NGS) adapter ligation and DNA sequencing by the Sanger method.

Used to eliminate carryover polymerase chain reaction (PCR) products in qPCR and RT-qPCR,by incorporating dUTP in reactions, so residual products from previous PCR amplifications containing dUs can be digested.

Used to eliminate carryover polymerase chain reaction (PCR) products in qPCR and RT-qPCR,by incorporating dUTP in reactions, so residual products from previous PCR amplifications containing dUs can be digested.

Very high yield, high-performance polymerase, to give fast, superior amplification, even with challenging templates and in the presence of PCR inhibitors.

Mix of anti-Taq monoclonal antibodies designed to block Taq DNA polymerase activity at room temperature. Used in the preparation of hot-start PCR or qPCR master mixes.