4-Methylumbelliferyl-α-L-iduronic acid, cyclohexylammonium salt

(4-Methylumbelliferyl-α-L-iduronide; 4-MU-α-L-IdoA CHX)

Molecular Biology Grade

Fluorogenic soluble enzyme substrate for α-L-iduronidase. α-L-iduronidase is deficient in the genetic disorder Mucopolysaccharidosis type I, also called Hurler syndrome. Diagnosis of Hurler syndrome involves enzymatic assay of α-L-iduronidase activity using the fluorogenic enzyme substrate 4-Methylumbelliferyl-α-L-iduronide.

Off-white powder

Store at -15°C in a dark, dry place.

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