NEXTflex Bisulfite-Seq Kit for NGS Methylome Analysis Launched

13 Aug 2012
Tesni Perry
Administrator / Office Personnel

Product news

Today Bioo Scientific announced the launch of the NEXTflex™ Bisulfite-Seq Kit which is the first complete kit available designed to simplify library preparation of bisulfite treated DNA for down-stream high-throughput sequencing. Bisulfite-seq is an important method for studying DNA methylation and epigenetic gene regulation as it allows for an unbiased genome-wide analysis of DNA methylation generating a high-accuracy methylome.

NEXTflex™ Bisulfite-Seq Kit is designed to work with reduced representation or total bisulfite-converted DNA libraries and is compatible with single, paired-end and multiplexed DNA libraries on Illumina® MiSeq, GAIIx and HiSeq platforms. It includes Bioo Scientific’s proprietary “Enhanced Adapter Ligation Technology” which offers improved ligation efficiency than other commercially available solutions resulting in library preps with a larger number of unique sequencing reads. This kit also uses a completely gel-free protocol making the workflow compatible with liquid handler automation. For multiplexing, NEXTflex™ Bisulfite-Seq Barcodes can be purchased separately.

Bioo Scientific has also launched the NEXTflex™ Msp1 Restriction Enzyme, which unlike other commercially available Msp1 restriction enzymes, has been optimized for bisulfite sequencing.

According to Dr. Masoud Toloue, Director of Genomic Research at Bioo Scientific, “Short of direct sequencing of methylated cytosines, Bisulfite-Seq is currently the most sensitive and accurate method of elucidating epigenetic marks, the NEXTflex kit is designed to get you there.”

The NEXTflex™ Bisulfite-Seq Kit and Barcodes are the latest addition to Bioo Scientific’s line of innovative kits for next generation sequencing library preparation and, like our other library prep kits, the NEXTflex Bisulfite-Seq Kits are all available for next day delivery.

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Genome AnalysisGenomics, the study of genomes, includes functional genomics, evolutionary genomics and comparative genomics. There are many genomic technologies such as DNA sequencing of whole genomes, computational biology and bioinformatics. DNA and nucleic acids must be isolated and concentrated from cells for analysis with kits, automated analyzers and software. Other useful technologies for studying genomics include PCR, microarrays and electrophoresis.High-Throughput ScreeningHigh-throughput screening (HTS) is an automated drug discovery technique for identification of active compounds against a compound library. Use HTS readers and integrated assay preparation / analysis workstations to screen your compounds. Identify active compounds against various HTS libraries, including membranes, proteins and peptides and HTS cell lines. Find the best high-throughput screening products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.DNA SequencingDNA sequencing, such as sanger sequencing, is a biological technique that determines the precise order of nucleotide bases in a fragment or template of DNA. DNA sequencers and genetic analyzers are based on capillary electrophoresis, where labeled DNA fragments are electrophoretically separated by size as they migrate through a polymer. Find the best DNA sequencing products, including DNA sequencing kits, genomic libraries and genetic identity kits in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Next Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.DNA Methylation
NEXTflex Bisulfite-Seq Kit for NGS Methylome Analysis Launched