A simple method has been developed for the partial purification of arylsulphatase B from sheep brain. This includes concanavalin A‐Sepharose affinity chromatography and ionic strength‐dependent binding and dissociation of the enzyme with Dextran Blue; by these methods the enzyme was purified 1344‐fold with 10% recovery. The partially purified enzyme was shown to be a glycoprotein and its kinetic properties were compared with that of purified arylsulphatase A from the same source.
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Balasubramanian et al. (1976) studied this question.
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