Summary:1. Two methods for the Separation and Demonstration of creatine kinase isoenzymes are described i.e. electrophoresis on cellulose acetate and on electroendosmosis-low agarose.2. The fluorescence of NADPH äs an indicator for the creatine kinase bands was used in both methods.3. The methods proved to be specific, reliable and highly reproducible, and allow a rather large number of samples (12 -18) to be anälysed in one run within a relatively short time.