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 homology with human arylsulfatases A, B, and C, and human glucosamine-6-sulfatase. A splice variant of this gene has been described.
![Western Blot Iduronate 2-Sulfatase/IDS Antibody [Unconjugated]](http://images.novusbio.com/fullsize2/IDS_AF2449_Immunoprecipitation_19303.jpg)
![N/A Iduronate 2-Sulfatase/IDS [Biotin]](http://images.novusbio.com/fullsize2/DATA_IDS_DY244905_ELISA_2395.jpg)
