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Accel-NGS™ 2S DNA Library Kit for Illumina  
Swift Biosciences, Inc.

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For the Preparation of DNA Libraries for Next Generation Sequencing (NGS) on Illumina Platforms. The new Accel-NGS 2S DNA Library Kit for Illumina utilizes a proprietary adapter...
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Accel-NGS™ 2S XT Compatibility Module  
Swift Biosciences, Inc.

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Adapter and pre-hyb PCR primers for preparing DNA libraries for SureSelectXT hybridization and sequencing on the Illumina system.
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Uncloned Normalized cDNA for Next-Generation Sequencing  
Bio S&T

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Our uncloned normalized cDNA is created using proprietary technology which features full-length-enriched and high quality size-fractionated cDNA. Our cDNA has been used successfully with...
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InView™ Microbiome Profiling 2.0  
GATC Biotech

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Highlights: Multiplexing of up to 96 samples Increased amplicon length applying 2 x 300bp paired-end sequencing mode Optimised bioinformatics pipelines for samples of any...
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Accel-NGS™ 1S DNA Library Kit for Illumina  
Swift Biosciences, Inc.

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For the Preparation of DNA Libraries for Next Generation Sequencing (NGS) on Illumina Platforms. Based on innovative Swift technology, the Accel-NGS 1S DNA Library Kit for Illumina...
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Normalized cDNA libraries  
Bio S&T

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Our cDNA libraries feature full-length-enriched and high quality size-fractionated cDNA. cDNA library construction is usually done in slightly-modified versions of pBluescript or pcDNA3.1.
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InView™ Human Exon  
GATC Biotech

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Highlights: Fast access within 10 business days, starting from one sample Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample) Special...
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Accel-NGS™ DNA Library Kit for Ion Torrent  
Swift Biosciences, Inc.

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For the Preparation of DNA Libraries for Next Generation Sequencing (NGS) on Ion Torrent Platforms. Based on innovative Swift technology, the Accel-NGS DNA Library Kit for Ion Torrent...
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InView™ Transcriptome  
GATC Biotech

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Highlights: Highly standardised Scaled to fit any application and need Guaranteed output of read numbers per package InView™ stands for streamlined high-quality next...
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SPRIworks Fragment Library System I for Illumina Genom...  
Beckman Coulter

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Fully Automated Fragment Library System for the Illumina* Genome Analyzer The emergence of second generation sequencing technologies has enabled scientists to generate vastly increased...
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HaloPlex Custom Kits  
Agilent Technologies

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HaloPlex custom kits provide you the flexibility to perform pilot studies and easily increase your throughput. Scale up to 96 samples prepped in less than a day with Agilent automation. •...
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SureSelect Custom DNA  
Agilent Technologies

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Agilent’s market leading SureSelect platform provides a complete portfolio of catalog and custom products, providing the flexibility you need from discovery to follow-up studies. Agilent’s...
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SureSelect Custom RNA  
Agilent Technologies

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Agilent’s market leading SureSelect platform provides a complete portfolio of catalog and custom products, providing the flexibility you need from discovery to follow-up studies. Agilent’s...
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SureSelect DNA Capture Arrays   
Agilent Technologies

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Designed for smaller studies, the SureSelect DNA Capture Arrays complement Agilent's in-solution SureSelect Target Enrichment System, which is designed for medium to large-scale NGS studies...
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SureSelect DNA Panels  
Agilent Technologies

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Agilent SureSelect DNA panels are predefined designs which focus on targeted gene sets for specific applications. Agilent offers two human panels, the SureSelect Human Kinome panel and...
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SureSelect Strand Specific RNA Library Preparation Kits  
Agilent Technologies

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Agilent's SureSelect Strand Specific RNA Library Preparation Kit is the highest sensitivity, strand-specific method for preparing libraries for mRNA or targeted RNA-seq, enabling a greater...
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SureSelect Target Enrichment System Kit  
Agilent Technologies

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Agilent's SureSelect market leading platform provides a complete portfolio of catalog and custom products, providing the flexibility you need, for your discovery to follow-up studies. ...
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Magna ChIP-Seq™ Chromatin Immunoprecipitation and Next...  
EMD Millipore, a division of Merck KGaA, Darmstadt, Germany

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ChIP-Seq facilitates genome-wide profiling of the interactions of transcription factors, modified histones, and other chromatin associated proteins. By combining chromatin...
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SPRIworks Fragment Library System II for Roche GS FLX ...  
Beckman Coulter

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Fully Automated Fragment Library System for the Roche* 454 GS FLX DNA Sequencer The emergence of next generation sequencing technologies has enabled scientists to generate vastly...
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SPRIworks Fragment Library System III for Life Technol...  
Beckman Coulter

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Fully Automated Fragment Library System for the Life Technologies SOLiD* Sequencer The SPRIworks Fragment Library Systems have built-in size selection and prepare fragment libraries...
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GeneRead DNAseq Library Quant Array  
QIAGEN

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PCR Array format for QC of target enrichment process and quantification of DNA library in GeneRead DNAseq Gene Panel application
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Sample Library Construction Kits  
AMSBIO

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AMSBIO's Sample Library Construction Kits reduce NGS workflow complexity, shorten sample library preparation time and labour, and minimise errors by eliminating extra steps and optimising...
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ACSIA NGSCapture Edition  

4 out of 5


PrimaDiag

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ACSIA NGS Capture Edition, the solution to automate the steps of library preparation and, more specifically, of target enrichment. ACSIA NGS Capture Edition allows you to perform 48...
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  • Ease of use 5 out of 5
  • After sales service 4 out of 5
  • Value for money 4 out of 5

1 review(s) of this product / read all

ACSIA NGSLibPrep Edition  
PrimaDiag

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ACSIA NGS LibPrep Edition, the solution to automate the libraries preparation for next-generation sequencing. In view of increasing your productivity, avoiding contamination and...
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HaloPlex Cancer Research Panel  
Agilent Technologies

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The HaloPlex Cancer Research Panel enables fast, simple, and efficient analysis of genomic regions of interest for cancer research for a large number of sample types, including FFPE. ...
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