This technique is widely used in laboratories, especially in those of molecular biology, because it is used in important procedures such as: separation, analysis and purification of RNA, DNA, or proteins, nucleic acids, this process is performed because most biomolecules have an electrical charge where their magnitude depends on the pH of the medium in which they are found; because of this, the biomolecules move when subjected to an electric field to the charge pole opposite to that of the molecule.
Its operation is a simple process, separates the molecules according to their size and electrical charge, for this an electric current is used that impels to displace the molecules through a gel or another matrix., then the pores of the gel act as a sieve, allowing the smaller molecules to move faster than the larger molecules, to know the size of the molecules in a sample, they are compared with the established size standards that are separated into the same gel.