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Developing a 43 color panel on Cytek Aurora using Laminar Wash for sample prep

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Successfully executing a 43 color panel is a technically demanding task. One that is made more difficult when there are...

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Extracellular Vesicle Purity Enhanced by Gen 2 qEV Columns With Customised Proprietary Resin

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Why use Cytek Aurora?

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A prodigy incorporating a unique combination of patent-pending innovative technologies that takes flow cytometry to the...

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Introducing Celloger Mini Plus: Automated and compact Live cell imaging inside your incubator

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Linked-read sequencing advances understanding of cancers

Jul 8, 2019

A new study from the University of Connecticut Medical School, Jackson Labs, and collaborators demonstrate the utility of using emulsion based linked-read sequencing for cancer research.From a methods standpoint, linked-read sequencing requires only 1 ng of DNA input and produces haplotype phasing information. With a 1 ng input requirement, there is ample recovery in the PippinHT – users simply quantify the sample with a Qubit fluorometric assay, and dilute the sample accordingly. On a side note, SageHLS platform has the capability to provide very large targeted genomic regions, a great application for linked-reads given the low input requirement.

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Sage Science

Preparative electrophoresis systems for targeted size selection of biomolecules.

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Targeted Size Selection for Next-Gen Sequencing (90bp – 1.5kb)

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Targeted Size Selection for Next-Gen Sequencing (90bp – 50kb)

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Automated size selection for 24 samples at a time.

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Whole Sample Fractionation of DNA or Protein - Collect 12 Contiguous Fractions from a Single Sample

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