Human SGCE ELISA Kit (HUFI06570)

Quantitative measurement of epsilon-sarcoglycan (SGCE), a transmembrane glycoprotein encoded on chromosome 7q21, supports research into myoclonus-dystonia syndrome (DYT11), a movement disorder where loss-of-function mutations disrupt this component of the dystrophin-associated protein complex.

The colorimetric ELISA Kit from Assay Genie is configured for human specimens, with reagents supplied for 96 individual assays in microplate wells. Investigators studying dystonia pathophysiology, maternally imprinted expression patterns, sarcoglycan family regulation, and neuronal membrane biology will find this kit useful for circulating biomarker quantification in translational neuroscience research.