Human Iduronate-2-Sulfatase (IDS) ELISA Kit

Iduronate-2-Sulfatase (IDS) is a lysosomal sulfatase essential for the stepwise catabolism of glycosaminoglycans such as heparan sulfate and dermatan sulfate. Deficiency of this enzyme causes Hunter syndrome (MPS II), an X-linked lysosomal storage disorder in which undegraded substrates progressively accumulate in tissues. Assay Genie offers this ELISA kit for the quantitative measurement of IDS protein in human specimens, supporting work in disease mechanism studies, biomarker validation, and monitoring of enzyme replacement therapy outcomes.

This 96-assay format kit employs an absorbance-based colorimetric method compatible with standard microplate readers, with all necessary reagents supplied for the full plate workflow. It is intended for research use only and is validated for use with human-derived samples, including applications in lysosomal storage disorder research, clinical biomarker studies, and biochemical characterization of sulfatase activity.