How are DNA fragments separated in gel electrophoresis?

DNA gel 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.

DNA fragments have a net negative charge; when subjected to an electric field, the negatively charged nucleic acid fragments migrate towards the positive electrode. The length of DNA fragments is a primary factor that influences the rate of migration—shorter DNA fragments travel faster through the gel matrix than longer fragments. Therefore, DNA gel electrophoresis results in separation—or resolution—of DNA fragments based on size.

Thermo Fisher Scientific provides high-quality gels, reagents, and devices to support the DNA electrophoresis workflow.

To craft a gel of choice, use UltraPure agarose powder or UltraPure acrylamide powder; these high quality gels allow for superior resolution and the formation of sharp bands. Agarose gels can also be cast with TopVision agarose tablets.





Resources

Nucleic acid electrophoresis products
Explore Thermo Fisher Scientific’s suite of products for all your electrophoresis needs.

Nucleic acid electrophoresis education
Learn about gel electrophoresis basics, workflow, considerations, applications, and troubleshooting for separation and analysis of nucleic acids.

DNA and RNA protocols
Find easy-to-follow protocols for everyday experiments, including agarose protocols and mRNA protocols.

Support

Nucleic acid purification and analysis support center
Find tips, troubleshooting help, and resources for your nucleic acid purification and analysis applications.

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