Anti-HEXA antibody

Polyclonal

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

P06865

This gene encodes a member of the glycosyl hydrolase 20 family of proteins. The encoded preproprotein is proteolytically processed to generate the alpha subunit of the lysosomal enzyme beta-hexosaminidase. This enzyme, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene lead to an accumulation of GM2 ganglioside in neurons, the underlying cause of neurodegenerative disorders termed the GM2 gangliosidoses, including Tay-Sachs disease (GM2-gangliosidosis type I). Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed.

HEXA

Rabbit polyclonal against HEXA

Calculated: 19kDa/60kDa.

Anti-Beta-Hexosaminidase Subunit Alpha antibody
Anti-Beta-N-Acetylhexosaminidase Subunit Alpha antibody
Anti-Hexosaminidase Subunit A antibody
Anti-N-Acetyl-Beta-Glucosaminidase Subunit Alpha antibody
Anti-HEXA antibody

FOR RESEARCH USE ONLY (RUO).