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SPRIworks Fragment Library System I  
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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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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Fragment Library  
ChemBridge Corporation

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A collection of approximately 5,000 compounds rationally selected according to various diversity parameters and Astex Rule of Three considerations (MW ≤ 300, H-bond donors ≤ 3, H-bond...
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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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DEMO KIT: SureSelect Human X Chromosome  
Agilent Technologies

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Agilent™s SureSelect Target Enrichment System is a highly efficient hybrid selection technique for optimizing next-generation sequencing. It is available for the Illumina GA and...
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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 Target Enrichment Kits   
Agilent Technologies

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Agilent's new SureSelect platform allows you to focus your next-gen sequencing workflow on key genomic regions of interest while reducing cost per sample. As the leading provider of target...
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SureSelect Target Enrichment System Kit  
Agilent Technologies

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Agilent™s SureSelect Target Enrichment System is a highly efficient hybrid selection technique for optimizing next-generation sequencing. It is available for the Illumina GA and...
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SureSelect XT Kits   
Agilent Technologies

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SureSelectXT Kits offer a complete target enrichment workflow for next-generation sequencing. SureSelectXT Kits contain a SureSelect Target Enrichment Kit along with an optimized gDNA prep...
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PureGenome™ On-Spot Tissue DNA Kit  
EMD Millipore, a division of Merck KGaA, Darmstadt, Germany

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The PureGenome™ On-Spot Tissue DNA kit allows for convenient isolation of genomic DNA in any targeted microscopic tissue area on a slide. The system combines a powerful area-specific...
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PureGenome™ Tissue DNA Extraction Kit  
EMD Millipore, a division of Merck KGaA, Darmstadt, Germany

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The PureGenome™ Tissue DNA Extraction Kit is a simple procedure for the rapid isolation of total DNA (e.g. genomic, mitochondrial, parasitic, microbial, viral) from a variety of soft and...
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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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PGN001 PureGenome™ Next Generation Sequencin...  
EMD Millipore, a division of Merck KGaA, Darmstadt, Germany

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The PureGenome™ High Efficiency Next Generation Sequencing (NGS) Library Preparation Reagents are uniquely optimized as a one-stop solution for NGS Library Preparation. Validated for...
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PGN003 PureGenome™ Next Generation Sequencing...  
EMD Millipore, a division of Merck KGaA, Darmstadt, Germany

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The PureGenome ™ High Efficiency Next Generation Sequencing (NGS) Library Preparation Reagents are uniquely optimized as a one-stop solution for NGS Library Preparation. Validated for...
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PGN004 PureGenome™ Next Generation Sequencing...  
EMD Millipore, a division of Merck KGaA, Darmstadt, Germany

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The quality of sequence obtained from Next Generation sequencing platforms such as Illumina, Inc. requires the accurate determination of input library DNA. Loading too much DNA can lead to...
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Reverse Transfection Format (RTF) siRNA Libraries  
Thermo Fisher Scientific

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Standard siRNA libraries require multiple aliquoting steps that can introduce variability and contamination in the absence of appropriate handling systems. Thermo Scientific Reverse...
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Sample Library Construction Kits  
AMS Biotechnology

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AMSBIO's S ample 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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VERSA Next Generation Library Preparation Workstation  

5 out of 5


Aurora Biomed

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Next generation sequencing (NGS) technologies are emerging as a powerful means for providing gigabases of genetic information in a single run. The increase in throughput and reduction in...
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  • Ease of use 4 out of 5
  • After sales service 5 out of 5
  • Value for money 5 out of 5

1 review(s) of this product / read all

Fosmid Library  
Bio S&T

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We use a proprietary physical random shearing and cloning method to produce unbiased fosmid libraries. The pCC1Fos copycontrol vector will also facilitate production of fosmid DNA.
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RNA Isolation for Sequencing  
Bio S&T

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Bio S&T's high-quality RNA can be used directly for NxGen RNA sequencing as well as other downstream applications that require optimal-quality RNA such as quantitative real-time...
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Fragment Library  
ChemBridge Corporation

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ChemBridge has assembled an exemplary collection of small molecules useful for fragment-based screening: the Fragment Library. The emergence and development of high throughput X-ray...
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Bioruptor® Pico  

5 out of 5


Diagenode

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The Bioruptor® Pico is the latest innovation in shearing and represents a new breakthrough as an all-in-one shearing system optimized for shearing micro-volumes of 5 ul to larger volumes of...
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  • Ease of use 5 out of 5
  • After sales service 5 out of 5
  • Value for money 5 out of 5

1 review(s) of this product / read all

True MicroChIP Kit and MicroPlex Library Preparation K...  
Diagenode

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The True MicroChIP Kit and MicroPlex Library Preparation Kit provide a powerful combination of chromatin immunoprecipitation from 10,000 cells and next-generation sequencing library...
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Ion AmpliSeq™ Cancer Panel  
Life Technologies

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The Ion AmpliSeq™ Cancer Panel provides a fast & easy, cost effective sequencing workflow for single-tube preparation of amplicon libraries from genomic "hotspot" regions that frequently...
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