Products & Reviews

EpiScript™ Rnase H- Reverse Transcriptase (EpiScript RT) is a recombinant MMLV reverse transcriptase with greatly reduced RNase H activity. It is highly efficient at producing full-length cDNA from long RNA templates. EpiScript RT is capable of producing cDNA from as little as 50 pg of total RNA for real-time RT-PCR (qRT-PCR) analysis and other applications.

Formulated with diagnostic kit developers in mind, RapiDxFire™ qPCR 5X Master Mix glycerol free (GF) can be combined with gene-specific primers and hydrolysis probes for immediate use in high-throughput laboratory developed test (LDT) workflows or further processed for lyophilisation for use in point of care (POC) devices. Provided at a 5X concentration without passive reference dye, this flexible master mix allows more room…

The Soellex™ is an ultra-high-throughput end-point PCR thermal cycler leveraging a 3-chamber water bath.

Rapid fluorescence detection for PCR and isothermal amplification. The Araya is a top-read fluorescence detector.

The Yale 2019-nCoV SalivaDirect™ ValuPanel Reagents™ include FAM-BHQ and Quasar™ 670-BHQ probes and primers delivered in individual tubes in dried format.

A dual-labelled probe that combines a hairpin structure and a PCR primer element in a single oligo, allowing for target detection through a unimolecular mechanism. Mismatched hybrids are less stable than the reformed stem region. Therefore, Scorpions Primers only produce signal when the probe region hybridizes to a perfect-match target sequence within the primer extension product. 

Consistent, high-quality beads for single-cell mRNA sequencing applications using Drop-Seq methods  

Choose premier KASP on Demand (KOD) service for design and delivery of your KASP Assay, plus full validation and optimization of your assay by our scientific team.  

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.  

Licence-free MGB probes for any application

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

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.