Iduronate 2 Sulfatase Mouse anti-Human, Mouse, Clone: OTI1D9, Invitrogen
Mouse Monoclonal Antibody
Manufacturer: Invitrogen MA525855
DescriptionIduronate-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.
|Iduronate 2 Sulfatase|
|PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3|
|IDS; iduronate 2-sulfatase (Hunter syndrome); MPS2; SIDS; iduronate-2-sulfatase|
|-20° C, Avoid Freeze/Thaw Cycles|
|Flow Cytometry, Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot|
|Full length human recombit protein of IDS produced in HEK293T cell|
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