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GLA
Galactosidase alphaGALA
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]
Top validated antibodies |
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| Proteintech Group |  15428-1-AP |
2 references | Polyclonal |
WB
EL
IP
IHC
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| antibodies-online | ABIN551188 |
4 references | Polyclonal |
WB
IP
IHC
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| Invitrogen Antibodies | PA5-27349 |
3 references | Polyclonal |
WB
IHC
OA
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| Abgent | AP6727A |
Polyclonal |
WB
ICC
IHC
FC
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| GeneTex | GTX101178 |
1 references | Polyclonal |
WB
IP
IHC
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