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In biolaboratories, agarose gel electrophoresis is the modus operandi for size-based separation of DNA and RNA fragments. The agarose gel matrix is porous and acts as a sieve through which the nucleic acid molecules migrate.

Nucleic acid electrophoresis is a standard laboratorytechnique that underpins molecular biology research. Traditionally, gel electrophoresis takes a lot of time and involves casting the gel, making buffers, preparing samples and ladders, loading and running the gel,as well as visualizing and imaging...

Note : When placing the E-Gel 96 bases on a Biomek Automated Labware Positioner (ALP), position the bases in the upper right corner of the ALP. This will allow the Biomek to reliably access the E-Gel 96 system. A demonstration method, E-Gel Demo.

Electrophoresis is a common lab technique used to identify, quantify, and purify nucleic acid fragments and assess quality. RNA molecules are negatively charged, and during gel electrophoresis they migrate toward the anode in the presence of an electric current.

The E-Gel Power Snap Electrophoresis System is a compact, precast agarose gel running and imaging station saving time and bench space. It requires no connection to a desktop computer, so you can run gels and capture images on the spot.

The busy scientist Benefits of using modern methods Maximizing your time with high quality systems and consumables, In his 1748 essay “Advice to a Young Tradesmen,” Ben Franklin made what is now the timeless statement that “Time is money.

DNA electrophoresis is a standard laboratory technique used to identify, quantify, and purify DNA fragments. DNA electrophoresis involves loading DNA samples into the wells of an agarose or acrylamide gel and subjecting it to an electric field.

Gel electrophoresis is a common laboratory technique to isolate nucleic acids and proteins. Nucleic acid electrophoresis uses a gel matrix to separate DNA and RNA fragments based on size and molecular weight. Gel electrophoresis is vital in all molecular biology workflows.

E-Gel precast gels are bufferless agarose gels with electrodes embedded in the agarose matrix. Each precast agarose gel contains an ion generating system, a pH balancing system, and DNA stain packaged inside a transparent plastic cassette.

Learn about the basics and tips on gel electrophoresis for nucleic acid separation and analysis. Find technical resources on nucleic acid gel electrophoresis, covering the history, setup, workflow, considerations, applications, and troubleshooting.

In the nucleic acid electrophoresis workflow, several steps are performed sequentially, each of which could impact the outcome of nucleic acid separation. This article addresses five considerations associated with samples, reagents, and running parameters.

Most life science researchers will run a gel at some point in their careers. Running a gel, formally called gel electrophoresis, is an effective method to separate biomolecules, such as nucleic acids and proteins , based on size.

Nucleic acid electrophoresis uses a gel matrix to separate DNA and RNA fragments based on size and molecular weight. In blotting, DNA and RNA fragments, separated by electrophoresis, are transferred to a membrane matrix.

Perform agarose gel electrophoresis of nucleic acids using tanks, combs, power supplies, and other accessories of Thermo Scientific™ Owl™ Horizontal Gel Electrophoresis Systems. Choose among the following format series: large (A1-A6), micro (C2-S), wide (D2-D4), and mini (EasyCast™ B1-B3).

For Research Use Only. Not for use in diagnostic procedures., View all How do I decide which percentage gel to use? I’d like to isolate DNA after gel electrophoresis. What do you recommend? How much DNA can I load for my E-Gel® Agarose Gels? How can I perform RNA electrophoresis?