Human Glucosidase Alpha, Acid (GaA) ELISA Kit

Quantitative measurement of acid alpha-glucosidase (GAA) in human specimens is supported by this ELISA Kit from Assay Genie. GAA is a lysosomal hydrolase responsible for glycogen breakdown, and deficiencies in its activity are the molecular hallmark of Pompe disease (glycogen storage disease type II). Reliable quantification matters for research into metabolic and neuromuscular disorders, including studies of enzyme replacement therapy response and genetic deficiency models.

Provided as a complete kit with all reagents needed to run the immunoassay, including precoated plate, specific antibodies, protein standards, assay buffers, wash solution, and substrate. The kit accepts a range of specimen types, including blood-derived samples, tissue homogenates, and cell lysates, accommodating workflows from cell-based models to clinical sample analysis.

For research use only. Store unopened components refrigerated and protect from light; reconstituted reagents should be aliquoted to limit freeze-thaw cycles. Each kit supplies material for 96 individual determinations in a microplate layout, supporting both small-scale pilot studies and higher-throughput screening campaigns.