DNA Sequencing Products & Reviews

Whether your profiling experiment requires ultimate sensitivity, broad coverage or both, Megaplex™ Primer Pools provide the flexibility to reach your research goals. Megaplex Primer Pools deliver comprehensive coverage of Sanger miRBase v10, and when used with TaqMan® MicroRNA Arrays, offer an ideal miRNA profiling solution. Optional Megaplex™ PreAmp Primers significantly enhance the ability to detect low expressed miRNAs en…

We set a new standard in capillary electrophoresis with the 8-capillary 3500 and 24-capillary 3500xL Genetic Analyzers. The 3500 8-capillary platform can run a wide variety of applications —including de novo sequencing and resequencing (mutational profiling)—as well as microsatellite analysis, MLPA™, LOH, MLST, AFLP® and SNP validation or screening. The majority of applications can be run on a single polymer and capillary arra…

Unlocking the potential of genomics with miniaturized, automated liquid handling 

All your genetic analysis needs on one instrument

Removal of unincorporated dye terminator after DNA sequencing reactions is a prerequisite to load samples on automated capillary sequencers. For rapid and effective removal of unincorporated dye terminator, Agencourt CleanSEQ® uses Solid Phase Reversible Immobilization (SPRIT) of DNA products on magnetic microparticles.

mRNA sequencing (mRNA-seq) is a potent method for gene expression exploration, it unveils mRNA dynamics, different gene expression and regulatory mechanisms with precision.

The Sciclone ® G3 NGSx workstation is a complete benchtop solution for the automated construction of up to or greater than 96 libraries per day.                  

With the Applied Biosystems 3130 Genetic Analyzer, you get the sophisticated automation and superior performance of the 3130 system, at acquisition and operating costs tailored to a growing research lab. Run a wide variety of sequencing and fragment analysis applications including microsatellite analysis, AFLP, LOH, SNP validation, and SNP screening. Reduce maintenance time by eliminating manual syringe washing and filling wit…

The 96-capillary 3730xl DNA Analyzer is the Gold Standard for high throughput genetic analysis. Use this for DNA fragment analysis applications such as microsatellites, AFLP, SNP analysis, mutation detection and traditional DNA sequencing. Get the highest quality data at a low cost per sample. Higher optical sensitivity and advanced polymers enable you to obtain higher-quality sequencing data for less. Multiple automation feat…

Biomek Liquid Handlers enable you can spend less time on manual process and more time on powerful discoveries. Beckman Coulter Life Sciences is a leader when it comes to providing solutions and support that cover the full spectrum of the NGS sample preparation workflow with reagents and automation. Throughput options allow you to choose the right solution for your laboratory.

Dominating the high-throughput sequencing data analysis challenge We have overcome the challenge to analyze high-throughput sequencing data faster than it is produced by implementing a SIMD-accelerated assembly algorithm in our next generation sequencing solution, CLC Genomics Workbench – a cross-platform desktop application with a graphical user-interface. CLC Genomics Workbench, for analyzing and visualizing next generation…

ACSIA NGSCapture Edition, the solution to automate the steps of library preparation and, more specifically, of target enrichment. ACSIA NGSCapture Edition allows you to perform 48 samples without human intervention or 96 samples with one intervention during the enrichment step. To do so, it operates from just after the hybridization up through the final PCR amplification. It is in this last step at the end of the process that…

The New Standard for Desktop-Based Bioinformatics Tools CLC DNA Workbench provides a software environment which enables users to perform advanced DNA sequence analyses such as assembly of DNA sequence data, graphically and algorithmically advanced primer design, while offering user-friendly molecular cloning tools. CLC DNA Workbench is a bioinformatics software package containing a range of specialized DNA analyses and bioinfo…

The Eurofins sequencing services provide you with the most flexibility for your samples in tubes and plates. Tube Sequencing Services Mix2Seq TubeSeq Service TubeSeq Lables Ready2Load Plate Sequencing Services PlateSeq Service PlateSeq Kits Ready2Load Plate Get your Mix2Seq Kit to benefit from the smartest sequencing solution for your DNA samples premixed with primer. Available as overnight and Non-overnigh…

For the rapid purification of sequencing extension products from reaction mixes

Exceptional Gene Silencing Specificity For Reliable Phenotypes

The dGTP BrilliantDye Cycle Sequencing Kit is optimized for sequencing through GT- and G-rich templates

DNA collection kits for research

End-to-end transcriptome sequencing services from RNA extraction to sequencing to bioinformatic analyses.

Eton provides the following sequencing services tailored to your specific research.

CD Genomics provides complete plasmid DNA sequencing service, and their improved bioinformatics pipelines are available to perform de novo assembly with no reference required.

VAHTS TM  DNA Clean Beads are based on the SPRI (Solid Phase Reverse Immobilization) principle and are suitable for DNA purification and fragment size sorting in the construction of high-throughput sequencing libraries. VAHTS TM DNA Clean Beads are compatible with various brands of DNA and RNA library building kits and the library building process reported in the literature. 

Get the most complete genomic information of any organism with whole genome sequencing (WGS). Macrogen Europe’s fast, high-quality WGS services provide the most comprehensive tool for detecting genetic abnormalities such as single nucleotide polymorphisms (SNPs), indels, copy number variation (CNV) and structural variants (SVs).

Bridging histology and genomics

Economical 2-component kit ideally suited for high throughput gene-expression studies