Product DemonstrationsLife Sciences

Tutorial: Creating a Fractionation Protocol on SageELF (Video 3)

16 Dec 2014
Tutorial: Creating a Fractionation Protocol on SageELF (Video 3)

This the third of a series of instructional video for users of the SageELF by Sage Science. The SageELF is a DNA and protein fractionator which uses electrophoresis to create up to 12 contiguous fractions from a biological sample.

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Sage Science

Sage Science develops game-changing instrument products for sale to the Life Sciences research and Diagnostic laboratory markets. Our mission is to provide new systems to streamline and improve sample preparation workflows.

Sage Science is privately-funded. It is headquartered and manufactures at the Cummings Center in Beverly, MA, USA.

The Company released the Pippin Prep DNA size selection system in 2010. The Pippin has since established itself as the premium platform for high quality library construction for next gen sequencing applications.

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SageELF Sample Fractionator for DNA and Protein

Sage Science

The SageELF is an automated, whole-sample fractionation system for NGS sample prep. SageELF, a whole-sample fractionation tool, is now shipping from Sage Science, developer of the Pippin automated DNA size selection system. The SageELF (short for Electrophoretic Lateral Fractionator) generates 12 contiguous fractions from a whole DNA sample, allowing scientists to generate libraries with multiple insert sizes from the same sample, which has applications in genome sequencing, structural variant detection, and identification of rare splice variants. This sample prep instrument will also be especially useful for preserving precious samples. Users simply load their sample, start the run, and pipette out the fractions later. Unlike in-gel digestion, in which some DNA fragments never leave the gel, the whole DNA sample is electrophoresed into the elution modules.Sage Science targets labor-intensive steps in the sample prep process where automation can offer improved precision and reproducibility. Precise size selection is critical for optimizing sequencing efficiency, improving genome assemblies, and reducing NGS project costs.Features: Make libraries with multiple insert sizes from the same sample Ideal for rare or precious samples Automated for precise, reproducible results Applications: Genome sequencing Structural variant detection Rare splice variant detection

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