Agarose Gel Electrophoresis for the Separation of DNA Fragments
University of California, Los Angeles
Abstract
Agarose gel electrophoresis is the most effective way of separating DNA fragments of varying sizes ranging from 100 bp to 25 kb(1). Agarose is isolated from the seaweed genera Gelidium and Gracilaria, and consists of repeated agarobiose (L- and D-galactose) subunits(2). During gelation, agarose polymers associate non-covalently and form a network of bundles whose pore sizes determine a gel's molecular sieving properties. The use of agarose gel electrophoresis revolutionized the separation of DNA. Prior to the adoption of agarose gels, DNA was primarily separated using sucrose density gradient centrifugation, which only provided an approximation of size. To separate DNA using agarose gel electrophoresis, the…
Citation impact
- FWCI
- 10.10
- Percentile
- 100%
- References
- 11
Authors
4Topics & keywords
- Agarose
- Gel electrophoresis of nucleic acids
- Electrophoresis
- Agarose gel electrophoresis
- DNA
- Gel electrophoresis
- Ethidium bromide
- Molecular-weight size marker
- Life below water