Gel electrophoresis

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Gel electrophoresis is a method used in laboratory settings to separate DNA, RNA, or protein molecules based on their size and charge. This technique is commonly used in molecular biology, biochemistry, and genetics laboratories.

Overview[edit | edit source]

Gel electrophoresis works by applying an electric field to a gel that contains the molecules of interest. The molecules will move through the gel at different rates depending on their size and charge, allowing them to be separated.

Process[edit | edit source]

The process of gel electrophoresis involves several steps:

  1. Preparation of the gel: The gel is typically made from agarose or polyacrylamide, which are substances that create a matrix through which the molecules can move.
  2. Loading the samples: The DNA, RNA, or protein samples are loaded into wells in the gel.
  3. Applying the electric field: An electric field is applied to the gel, causing the molecules to move through the gel. The direction of movement will depend on the charge of the molecules.
  4. Staining and visualization: After the electrophoresis is complete, the gel is stained to make the bands of molecules visible. The gel can then be photographed or otherwise recorded for further analysis.

Applications[edit | edit source]

Gel electrophoresis has a wide range of applications in the field of molecular biology and genetics. It is used in DNA sequencing, genotyping, mutation detection, and protein purification, among other things.

See also[edit | edit source]

References[edit | edit source]

Gel electrophoresis Resources
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