Human HEXA ELISA Kit (HUFI03955)

HEXA encodes the alpha subunit of lysosomal hexosaminidase A, the enzyme whose deficiency underlies Tay-Sachs disease (GM2 gangliosidosis), and this Assay Genie ELISA kit provides quantitative colorimetric measurement of human HEXA protein in serum or plasma specimens. Researchers studying lysosomal storage disorders, neurodegeneration biomarkers, and carrier screening use this 96-assay plate to profile HEXA expression in patient-derived samples and disease models. Each kit includes the pre-coated plate, conjugate, standards, and buffer reagents needed to run a complete ELISA; reagents must be stored refrigerated and protected from light to preserve enzymatic activity. Validation work has confirmed reactivity against human HEXA, supporting translational research into gene expression, enzyme replacement strategies, and genotype-phenotype correlations in affected families.