Automated Library Preparation



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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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Source BioScience Next Generation Sequencing  
Source BioScience

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Source BioScience are one of Europe’s leading providers of commercial sequencing offering services on the most prominent next generation sequencing platforms including the Illumina MiSeq...
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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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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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InView™ Human Exome  
GATC Biotech

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Highlights: Fastest exome sequencing, starting from one sample Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample) Special protocol for...
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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 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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Bioruptor® Pico  

4 out of 5


Diagenode

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The Bioruptor® Pico is the new next-generation all-in-one shearing device, highly optimized for DNA shearing for next-generation sequencing, chromatin shearing for ChIP-seq applications,...
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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

7 review(s) of this product / Read All

iDeal Library Preparation Kit  
Diagenode

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The iDeal Library Preparation Kit reliably converts DNA into indexed libraries for next-generation sequencing, with input amounts down to 5 ng. Our kit offers a simple and fast...
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MicroPlex Library Preparation™ Kit  

4 out of 5


Diagenode

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The easiest NGS Library preparation you will ever find! The MicroPlex Library Preparation™ kit is the only kit on the market which is validated for ChIP-seq and which allows the...
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  • Ease of use 4 out of 5
  • After sales service 3 out of 5
  • Value for money 4 out of 5

1 review(s) of this product / Read All

SX-8G IP-Star® Compact Automated System  
Diagenode

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Chromatin immunoprecipitation and DNA methylation assays followed by next generation sequencing is a powerful technique for generating genome-wide profiles of epigenetic modifications and...
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True MicroChIP Kit  

4 out of 5


Diagenode

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The True MicroChIP kit in combination with the MicroPlex Library Preparation™ kit allows for performing ChIP-seq on as few as 10,000 cells. This microChIP-seq assay has been validated with...
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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

2 review(s) of this product / Read All

JANUS NGS Express  
PerkinElmer, Inc.

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Sample preparation is the key to high quality data for nucleic acid sequencing. Protocols for benchtop sequencers are complex multi-step methods requiring precise execution. Errors...
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InView™ De novo Genome 2.0  
GATC Biotech

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Highlights: Ideal for small genomes Highest N50 fewer and larger contigs Minimum number of mis-assemblies Extremely long reads The cuttinge-edge sequencing...
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InView™ Epigenome  
GATC Biotech

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Highlights: Study your methylome with high-end conversion rate (≤ 99,9%) on true base level resolution Applicable for all organisms with 5-methylcytosines with flexible scaling...
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InView™ Modification Analysis  
GATC Biotech

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Highlights: Resolve strand-specific modifications at single-base resolution Simultaneous detection of sequence and epigenetic variants Hypothesis-free detection InView...
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NeoPrep Library Prep System  
Illumina

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The NeoPrep System is designed for the Illumina family of NGS sequencers and makes the market leading TruSeq and Nextera library prep workflows even easier. At the heart of the NeoPrep...
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KAPA Hyper Prep Kits  
Kapa Biosystems, Inc.

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The novel one-tube chemistry, optimally formulated and evolved enzymes enable higher yields of adapter-ligated library and lower amplification bias. This translates to higher library...
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AB Library Builder™ System  
Life Technologies

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The AB Library Builder™ System simplifies next-generation sequencing by providing a semi-automated solution for DNA fragment and RNA whole transcriptome library preparation for the SOLiD® 4...
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LabChip® XT  
PerkinElmer, Inc.

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Advanced Nucleic Acid Size Selection and Collection The LabChip XT fractionation system performs fast, automated nucleic acid fractionation accurately and reproducibly. The resulting...
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LabChip® XTe  
PerkinElmer, Inc.

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The LabChip XTe fractionation system performs fast, automated nucleic acid fractionation accurately and reproducibly. The resulting sample is tightly sized and is delivered in a sequencing...
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