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1. There is a permeable gel with a row of holes on one side.

2. Different DNA samples are placed in holes using pipette.

3. An electric current is sent through the gel, with the opposite side as positive (the DNA is negatively charged).

4. Since the larger parts of DNA cannot get far through the gel and the smaller parts can. Several bands will be formed on the gel.

5. The bands are visible under UV light

6. These bands can be used to compare genetic similarity to determine the parent/sibling.

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The gel typically used in electrophoresis experiments is agarose gel.


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Before gel electrophoresis, techniques like paper electrophoresis and agarose slab gel electrophoresis were used for separating and analyzing DNA or proteins. These methods were less efficient and had lower resolution compared to gel electrophoresis.


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The absence of bands in gel electrophoresis can be caused by factors such as improper loading of samples, insufficient DNA concentration, or issues with the gel or electrophoresis equipment.


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A. J. Houtsmuller has written: 'Agarose-gel-electrophoresis of lipoproteins' -- subject(s): Blood protein electrophoresis, Electrophoresis, Gel electrophoresis, Lipoproteins


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