Anti-GBA antibody produced in rabbit
Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
Anti-D-glucosyl-N-acylsphingosine glucohydrolase antibody produced in rabbit, Anti-Acid β-glucosidase antibody produced in rabbit, Anti-β-Glucocerebrosidase antibody produced in rabbit, Anti-Glucosylceramidase precursor antibody produced in rabbit, Anti-Imiglucerase antibody produced in rabbit, Anti-Alglucerase antibody produced in rabbit
GBA (glucosidase, β, acid) is a simple glycosphingolipid. It consists of three non-contiguous domains, with the active catalytic site located in domain III and a (β/a)8 (TIM) barrel. In mammals, it is hydrolyzed by the lysosomal enzyme. 1,4 mutation in GBA gene leads to several neurological diseases, such as Parkinson disease (PD) and type 1 Gaucher disease (GD). In GD, β-glucosidase activity is significantly low.
