Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked Mucopolysaccharidosis Type II, also known as Hunter Syndrome. Iduronate-2-sulfatase has a strong sequence similarity with human arylsulfatases A, B, and C, and human glucosamine-6-sulfatase. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described.
Alpha-L-iduronate sulfate sulfatase; IDS iduronate 2-sulfatase (Hunter syndrome) MPS2 SIDS iduronate-2-sulfatase; Iduronate 2-sulfatase; iduronate sulfatase; iduronate-2-sulfatase
Cat # 15557822
100 µg
Cat # 15955454
100 µL
Cat # 15985005
100 µg
Cat # 15965464
100 µL
Cat # 16817695
20 µL
Cat # 15547482
100 µg
Cat # 15576822
100 µL
Cat # 16807695
150 µL
Cat # 11337013
100 µg
Cat # 16568801
100 µL
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