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aspartic acid, glutamic acid) and positively charged (i.e. Proteins are comprised of the 20 common amino acids, which include both negatively charged (i.e. Thus, batteries have their cathode labeled as "+" and anode labeled as "-". If this terminal of the battery is being reduced, then it must be the cathode in the redox reaction within the battery. Reduction at this electrode of the battery must be occurring and is driving the oxidation at the anode of the external electrodes. Note that the electrons from the anode are going to the "+" terminal of the battery. Redox chemistry within the external power supply is driving the redox reaction at the electrodes. (1985) Wedge-shaped ultrathin polyacrylamide and agarose gels for isoelectric focusing. (1988) Analytical and preparative electrophoresis in a non-uniform electric field. (1986) The use of agarose wedge-gel electrophoresis for resolving both small and large naturally occurring plasmids. (1984) Uniformly spaced banding pattern in DNA sequencing gels by use of field-strength gradient. (1983)An agarose gel resolving a wide range of DNA fragment lengths. (1984) Field gradients improve resolution on DNA sequencing gels.

(1983) Nonlinear gel electrophoresis: an analogy with ideal fluid flow. (1982) Nonuniform field gel electrophoresis. (1990) Protein analysis using high-resolution two-dimensional polyacrylamide gel electrophoresis. (1983) Quantitative two-dimensional gel electrophoresis of proteins. (1978) Preparative immunoabsorption electrophoresis. (1976) Recovery of SDS-proteins from polyacrylamide gels by electrophoresis into hydroylapatite. linos Scientific Publishers, Oxford, pp 75–76. (1977) A new staining technique for proteins in polyacrylamide gels using Coomassie Brilliant Blue G250. (1995) in Structure in Protein Chemistry. (1968) Pore-limit electrophoresis on a gradient of polyacrylamide gel. (1967) Polyacrylamide gel electrophoresis across a molecular sieve gradient. (1996) Electrophoretic analysis of plasminogen activators in polyacrylamide gels containing sodium dodecyl sulfate and copolymerized substrates. (1987) Tricine-sodium dodecyl sulfatepolyacrylamide gel electrophoresis for the separation of proteins in the range from 1–100 kDa. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T. (1969) The reliability of molecular weight determinations by dodecyl-sulphate-polyacrylamide gel electrophoresis. (1968) The binding of sodium dodecyl sulphate to various proteins. Jnr (1967) Molecular weight estimation of polypeptide chains by electrophoresis in SDS-polyacrylamide gels. (Ed.) (1996) Capillary Electrophoresis in Analytical Biotechnology. (1993) Practical Capillary Electrophoresis. (1993) Capillary Electrophoresis:Principles and Practice. (Ed.) (1993) Capillary Electrophoresis: Theory and Practice. (1993) Capillary Electrophoresis of Small Molecules and Ions. (Ed.) (1993) Capillary Electrophoresis Technology.

(1992) Capillary Electrophoresis:Principles, Practice and Applications. (Eds.) (1992) Capillary Electrophoresis: Theory and Practice. Design of integrated discontinuous buffer systems for analytical and preparative fractionation. Steady-state moving-boundary systems formed by different electrolyte combinations. (1964) Starch gel electrophoresis–application to the classification of pituitary proteins and polypeptides. (1955) Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults. (1961) Agarose as an anticonvection agent in zone electrophoresis. 14th International Conference on Chemical Education, Brisbane, Australia.