A synthesized peptide derived from human Galactosidase alpha (GLA) (GLA)
规格:
50 µl/100 µl/200 µl
规格:
50 µl
产品价格:
¥1650.0
规格:
100 µl
产品价格:
¥2685.0
规格:
200 µl
产品价格:
¥4230.0
分子量:Calculated MW: 46kDa
Observed MW: 50KDa
细胞定位:Lysosome
稀释方法:WB 1:500 - 1:2000
总结:This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. [provided by RefSeq, Jul 2008]