HEXA

HEXA, also known as α-N-acetylglucosaminidase, is a crucial lysosomal enzyme responsible for decomposing GM2 ganglioside and maintaining the stability of the intracellular environment. Its specific structure confers unique catalytic activity, making it play an irreplaceable role in cell metabolism. Functional defects in HEXA can lead to the accumulation of GM2 ganglioside within cells, subsequently triggering genetic diseases such as Tay-Sachs disease and Sandhoff disease. Therefore, conducting in-depth research on the structure, function, and signaling pathways of HEXA is significant for understanding the pathogenesis of these diseases and searching for effective treatment methods.

Popular Product:

Human Beta-hexosaminidase subunit alpha(HEXA) ELISA kit

Validated Data

Typical Data

Code：CSB-E09661h

Size：96T/48T

Sensitivity：3.9 pg/mL

Detection Range：15.6 pg/mL-1000 pg/mL

These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.