Tissue expression
Cell line expression
Protein structure
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 |
|
antibodies-online | ABIN551188 | 4 references | Polyclonal |
WB
IP
IHC
|
|
Invitrogen Antibodies | PA5-27349 | 3 references | Polyclonal |
WB
IP
IHC
OA |
|
Abgent | AP6727A | Polyclonal |
WB
ICC
IHC
FC |
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NSJ Bioreagents | F54879 | Polyclonal |
WB
ICC
IHC
FC |
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Enhanced validation
Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Recommended by provider
Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Recommended by provider