Electrophoresis is used in laboratories to separate macromolecules based on their charges. The technique normally applies a negative charge called cathode so protein molecules move towards a positive charge called anode.[2] Therefore, electrophoresis of positively charged particles or molecules (cations) is sometimes called cataphoresis, while electrophoresis of negatively charged particles or molecules (anions) is sometimes called anaphoresis.[3][4][5][6][7][8][9]
Liquid droplet electrophoresis is significantly different from the classic particle electrophoresis because of droplet characteristics such as a mobile surface charge and the nonrigidity of the interface. Also, the liquid–liquid system, where there is an interplay between the hydrodynamic and electrokinetic forces in both phases, adds to the complexity of electrophoretic motion.[12]
^Kastenholz, B. (2006). "Comparison of the electrochemical behavior of the high molecular mass cadmium proteins in Arabidopsis thaliana and in vegetable plants on using preparative native continuous polyacrylamide gel electrophoresis (PNC-PAGE)". Electroanalysis. 18 (1): 103–6. doi:10.1002/elan.200403344.
^Lyklema, J. (1995). Fundamentals of Interface and Colloid Science. Vol. 2. p. 3.208.
^Hunter, R.J. (1989). Foundations of Colloid Science. Oxford University Press.
^Dukhin, S.S.; Derjaguin, B.V. (1974). Electrokinetic Phenomena. J. Wiley and Sons.