A comparison of Tris‐glycine and Tris‐tricine buffers for the electrophoretic separation of major serum proteins

Abstract

Abstract This paper compares different buffer systems for the electrophoretic separation of the five most abundant serum proteins on native‐PAGE gel and cellulose membranes. A modified Tris‐tricine system was shown to be superior for the separation of these serum proteins in a 7% m/v native‐PAGE gel as compared with the traditionally used Tris‐glycine and Tris‐tricine methods. This modified Tris‐tricine buffer system was also employed for the separation of serum proteins using a cellulose acetate membrane and very effective separation was observed as compared with the traditionally used Tris‐barbital and Tris‐glycine buffer systems.