In this article, we will consider how agarose gel electrophoresis works, how it can be interpreted and some of its purposes. Electrophoresis is a technique that uses electrical current to separate DNA ...

A MICROELECTROPHORETIC technique for fractionation of RNA has already been described 1. Further work showed that it was necessary to increase the resolution when microisolated RNA was subjected to ...

Both kits use a novel gel system of EMBER™ Ultra Precoated Agarose with EMBER™ Loading Dye to achieve the highest sensitivity available for agarose gel-based detection and analysis. EMBER™ Ultra ...

The Clarit-E series of horizontal gel units offers the most versatile solution for DNA and RNA agarose gel electrophoresis currently available. All units offer an unsurpassed combination of economy of ...

We have developed a simple and rapid system for the denaturation of nucleic acids and their subsequent analysis by gel electrophoresis. RNA and DNA are denatured in 1 M glyoxal (ethanedial) and 50% ...

The system speeds up electrophoresis by completely eliminating the need to pour gels, prepare buffers, and stain and destain gels after running. Samples are simply loaded either manually with a ...

This webinar reviews RNA electrophoresis workflows and provides insights, tips and tricks, as well as reference resources to help simplify and optimize success in your RNA electrophoresis work.

Staining for RNA is commonly done with EtBr on a denaturing gel after electrophoresis. However, denaturing gels can be complicated to prepare and involve handling hazardous reagents. RNA prestaining ...

Current methods for the determination of RNA quantity/quality/integrity are labor-intensive, costly, and often cannot deliver adequate information or analyze high numbers of samples. New developments ...