Products & Reviews

The mag™ kits use magnetic beads to purify DNA from a variety of sample types. They are a cost-effective solution for automated DNA extractions using magnetic particle handlers, as well as liquid handlers.  The protocol follows the common technology of binding the DNA to the mag beads, removing contaminations by salt and alcohol based wash buffers and a final eluation step.  

Designed with input from top molecular diagnostic assay manufacturers, the RapiDxFire Lyo-Flex 1-Step RT-qPCR 5x Master Mix supports the development of diagnostic devices and assays that meet healthcare provider and consumer demand for fast, accurate results. With consistent results in a liquid state at room temp or in a lyophilised state, this master mix will help you achieve predictable performance in unpredictable conditio…

Improve assay sensitivity and specificity with Locked Nucleic Acid oligonucleotides (LNA oligos). LNAs are modified RNA bases in which the ribose is “locked” with a methylene bridge, connecting the 2' oxygen atom to the 4' carbon atom, fixing it in the C3'-endo conformation.  

One single kit to quickly and reliably determine 18 different and clinically relevant steroids with only one extraction process.

Licence-free MGB probes for any application

A workhorse, high quality DNA ligase for joining blunt or cohesive ends of dsDNA or dsRNA.

Accelerating drug discovery with better oligos

Reliable hot start Taq DNA Polymerase for sensitive detection of low abundance target DNA. Ideal for standard end point PCR and qPCR applications. Available in Glycerol-free, Triton-free, and high concentration formulations.

Phosphoramidite for the incorporation of an abasic spacer internally or at the 5' end of an oligonucleotide.

Phosphoramidite used to incorporate a 5' biotin functionality, separated from the oligonucleotide by a photo-cleavable linker.

Phosphoramidite used to incorporate the cyanine-3 dye moiety into an oligonucleotide.

CPG for incorporation of an (otherwise unmodified) reverse (5' to 3') dT nucleobase at the 3' end of an oligonucleotide.  

You know what you’re looking for and we’re here to help you find it. Our highly qualified molecular biologists and PCR assay design experts act as an extension of your team, designing the best qPCR assay for your target of interest and experimental conditions.  

CPG used to add the non-fluorescent quencher BHQ-1 dye to the 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for the incorporation of a 2'-fluoro modified nucleobase at the 3' end of an oligonucleotide

CPG for the incorporation of a 2'-O-methyl modified ribo- nucleobase at the 3' end of an oligonucleotide.

CPG for the incorporation of an (otherwise unmodified) reverse (5' to 3') nucleobase at the 3' end of an oligonucleotide.

CPG used to incorporate the cyanine-5 dye moiety onto the 3'-end of an oligonucleotide.