Electrophoresis is one of several physicochemical methods for characterization of proteins. It is performed by passing a high-voltage current through a dilute solution or dispersion of the material to be examined and observing the migration of the charged particles. This technic characterizes a protein only in respect to its behavior within an electric field, under the specific conditions of the experiment. Certain other data may be obtained at the same time. It may be noted whether the material under analysis is "pure," or consists of several components; the isoelectric point of a substance may be determined by varying the pH. The speed of migration of the charged particles and their possible dissociation into components of different mobilities are dependent on the pH, ionic strength and specific conductivity of the solution and the field strength selected. Electrophoresis may be employed to isolate fractions of specific materials in a relatively pure form, as well as for their quantitative estimation.In 1937, Tiselius 166 improved the moving boundary apparatus and technic for electrophoresis (observation of the interface between the protein and a supernatant clear buffer of the same pH and conductivity) to the extent that readily reproducible results were obtained. The Tiselius apparatus was then used in many investigations to demonstrate specific changes in the protein patterns in certain disease processes. However, the abnormalities encountered were usually nonspecific, and great caution is advisable when attempting correlations between these patterns and specific pathologic conditions. Electrophoretic analysis is not necessary or desirable for routine clinical examination of body fluids for the following reasons: the high cost of the necessary equipment and specially trained personnel; the time required for the analysis of a specimen (only a few can be examined in one day); the need for photographic and developing procedures; and the necessity of drawing enlarged patterns for measurement of the relative areas. In most instances, accurate, rapid, chemical fractionation procedures are now available and preferable.7 ; 167 However, the terminology utilized for the major protein constituents of plasma is based on their electrophoretic differentiation.