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1. Principle of separation
Gel electrophoresis is one of the main techniques in molecular biology. The basic principle of this
technique is that DNA, RNA, or proteins can be separated by an electric field. In this case, the molecules
are separated based on the rate of displacement by the electromotive force in the gel matrix. The transfer
rate depends on the size of the molecule in question.
In principle, this technique is similar to chromatography: separating mixtures based on differences in
material nature. In gel electrophoresis, separation performed on a mixture of materials with different
electrical charge depending
The nucleic acid molecules are separated by an electric field in which the negative molecules will
migrate to the positive pole (anode). Displacement process is based on the molecular weight of the
molecule, where a smaller molecular weight molecules will then be able to move quickly.
The nucleic acid molecules are separated by an electric field in which the negative molecules will migrate to
the positive pole (anode). Displacement process is based on the molecular weight of the molecule, where a
smaller molecular weight molecules will then be able to move quickly.
References :
Barril, Patricia & Silvia Nates. 2010. Introduction to Agarose and Polyacrylamide Gel Electrophoresis
Matrices with Respect to Their Detection Sensitivities. Argentina : Instituto de Virologa Dr. J. M.
Vanella, Facultad de Ciencias Mdicas, Universidad Nacional de Crdoba, Crdoba.