hMeDIP-Sequencing (hMeDIP-Seq) Service
Active MotifComprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants
DNA 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.
Comprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants
Reliable detection of cancer-associated mutations in 597 genes from liquid biopsy samples
cGMP-Grade Solution of dNTPs Pretested in PCR- Two concentrations available: 10mM and 25mM
Rapid human ID STR assays for forensic casework, databasing and relationship testing.
The PowerPlex® 18D System is a multiplex STR system for use in database and paternity testing
For low-to-medium throughput NGS needs, the Zephyr ® G3 NGS workstation is a compact, semi-automated solution designed to construct up to 96 NGS libraries per day. This compact workstation is equipped with a highly precise, 96-channel pipetting head and includes an integrated gripper. Also included in this compact workstation is on-deck temperature and shaking options and a waste tip chute.
Targeted NGS library preparation, gene expression and genotyping. Increase productivity and efficiency with automated, cost-effective, and easy-to-use workflows for targeted DNA next-generation sequencing (NGS) library preparation, gene expression analysis and genotyping by allele-specific PCR.
Bionano Data Solutions™ includes a complete suite of hardware and software for end-to-end experiment management, analysis and bioinformatics processing, along with convenient web-based management and monitoring tools.
The MiSeq FGx is the first fully-validated next generation sequencing (NGS) solution designed specifically for the challenges of human genetic identification.
Automated, preparative gel electrophoresis systems, used for accurate and reproducible size selection/collection of DNA (or cDNA) fragments, for the preparation of libraries for next generation sequencing (NGS)
Don’t risk wasting your precious sequencing samples. Diagenode’s validated iDeal ChIP-seq kit for Histones has everything you need for a successful start-to-finish ChIP of histones prior to Next-Generation Sequencing. The complete kit contains all buffers and reagents for cell lysis, chromatin shearing, immunoprecipitation and DNA purification. In addition, unlike competing solutions, the kit contains positive and ne…
Tagmentation is a reaction where an enzyme (a transposase) cleaves DNA and incorporates sequencing adaptors at the ends of the DNA fragments in one step. In our ChIPmentation technology we combine chromatin immunoprecipitation and tagmentation in one streamlined workflow where the tagmentation step occurs directly on chromatin. The TAG Kit for ChIPmentation has been developed for researchers who would like to perform Ch…
Transform your laboratory productivity with nanoscale automation delivering substantial cost and operational savings for RNA-Seq library preparation.
The complete synthetic reference material D614G is a full-length synthetic genome encoding the D614G spike protein mutation with a T7 promoter and a poly(A) tail. Genome modifications and editing are available.
Synthetic 5kb RNA regions spanning the length of the SARS-CoV-2 genome (NC_045512). Provide coverage of 99.9% of the bases of the viral genome. Controls are supplied in 100 µL at a concentration of one million copies per microliter.
Synthetic 5kb RNA regions spanning the length of the SARS-CoV-2 genome (NC_045512). Provide coverage of 99.9% of the bases of the viral genome. Controls are supplied in 100 µL at a concentration of one million copies per microliter.
Synthetic 5kb RNA regions spanning the length of the SARS-CoV-2 genome (NC_045512). Provide coverage of 99.9% of the bases of the viral genome. Controls are supplied in 100 µL at a concentration of one million copies per microliter.
Smart One RT-PCR Master Mix is designed for all applications that require Reverse Transcription of RNA into cDNA and a subsequent PCR amplification. Only primers and sample RNA have to be added to the mix
Plasma-SeqSensei™ (PSS) CRC RUO Kit allows the highly sensitive and specific detection of mutations in circulating tumour DNA (ctDNA) from plasma of patients with colorectal cancer (CRC). The kit is based on the next-generation sequencing technology and covers key mutations of the MAPK signaling genes KRAS, NRAS and BRAF and the PIK3CA genes. These genes significantly contribute to the development of colorectal cancer and a…