Gel electrophoresis is a technique that separates pieces of DNA (or other biological molecules) by size.
Pieces of DNA in a test tube all look the same.
DNA Gel Electrophoresis
Gel electrophoresis separates pieces of DNA by size so that researchers can further analyze them
BURST Training Session
November 29, 2005
Once the DNA samples are loaded onto the gel, an electric current is applied to the gel.
DNA is negatively charged due to all the phosphate groups in the backbone of DNA.
Thus, DNA will move towards the positive electrode.
How does gel electrophoresis work?
First a gel is prepared. Gels are made of agarose, a seaweed extract similar to gelatin.
The finished gel has a consistency similar to very firm jello. This consistency offers resistance to the pieces of DNA as they try to move through the gel. The gel is prepared with wells at one end so that DNA samples can be loaded into the gel.
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- electrode
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direction of migration
Wells for loading samples
- electrode
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Side View
Side view
+ electrode
Top view
+ electrode
Top View
Top view
As the pieces of DNA move through the gel, they will meet with resistance. Larger pieces of DNA will have more difficulty moving through the gel than smaller fragments.
Thus, larger fragments will move slower than smaller fragments. This allows separation of all different sizes of DNA fragments.
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Here you can see the migration of different fragments of DNA over time. Lane 2 contains a small fragment only, lane 3 a large fragment only, and lane 4 both a small and a large fragment.
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Larger fragment
Smaller fragment
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Uses of DNA Gel Electrophoresis
Is my DNA still there?
Is my DNA completely cut?
Uses of DNA Gel Electrophoresis
Restriction mapping - where in your DNA do specific enzymes cut relative to one another?
Uses of DNA Gel Electrophoresis
Did I get a PCR