25 products were found matching "GeneID 3423"!

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human IDS. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IDS. Next,...

Protein function: Required for the lysosomal degradation of heparan sulfate and dermatan sulfate. [The UniProt Consortium]

0.5mg/ml if reconstituted with 0.2ml sterile DI water. Iduronate 2 sulfatase (IDS) is an enzyme associated with Hunter syndrome. IDS is involved in the lysosomal degradation of the glycosaminoglycans heparan sulfate and dermatan sulfate. Wilson et al.(1991) used an IDS cDNA clone to localize the gene to Xq28, distal...

0.5 mg/ml in 1X TBS, pH7.3, with 0.5% BSA (US sourced) and 0.02% sodium azide. Additional name(s) for this target protein: Iduronate 2-sulfatase Protein function: Required for the lysosomal degradation of heparan sulfate and dermatan sulfate. [The UniProt Consortium]

This gene encodes a member of the sulfatase family of proteins. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. This enzyme is involved in the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this gene are associated with the X-linked lysosomal...

Iduronate 2-sulfatase (IDS) is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations causing IDS deficiency in humans result in the lysosomal storage of these glycosaminoglycans and Hunter syndrome,an X chromosome-linked disease. An internal proteolytic cleavage occurs to produce...

Iduronate 2-sulfatase (IDS) is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations causing IDS deficiency in humans result in the lysosomal storage of these glycosaminoglycans and Hunter syndrome,an X chromosome-linked disease. An internal proteolytic cleavage occurs to produce...

Protein function: Lysosomal enzyme involved in the degradation pathway of dermatan sulfate and heparan sulfate. [The UniProt Consortium]

Iduronate 2-sulfatase (IDS) is a lysosomal exohydrolase belonging to the sulfatase family and is required for the degradation of the glycosaminoglycans heparan sulfate and dermatan sulfate. IDS is synthesized as a 550-amino acid precursor comprised of an N-terminal signal peptide and propeptide that are cleaved...

Protein function: Lysosomal enzyme involved in the degradation pathway of dermatan sulfate and heparan sulfate. [The UniProt Consortium]