Gel electrophoresis

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

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

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

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

• Polymerase chain reaction
• Southern blot
• Western blot
• Northern blot

References

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  Gel electrophoresis apparatus

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  Diagram of gel electrophoresis

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  Gel electrophoresis in DNA fingerprinting

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  SDS-PAGE electrophoresis

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  Gel electrophoresis insert comb

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  Glucose-6-Phosphate Dehydrogenase activity stain

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  PCR gel

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  SDS-PAGE