Human GLα Antibody Pair Set (E-KAB-0257)
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For research use only.
| Background |
GLA,also named as Melibiase,Agalsidase and Alpha-galactosidase A,belongs to the glycosyl hydrolase 27 family. It hydrolyzes terminal,non-reducing alpha-D-galactose residues in alpha-D-galactosides,including galactose oligosaccharides,galactomannans and galactolipids. Fabry disease is an X-linked lysosomal storage disorder resulting from the deficient activity of GLA. Enzyme replacement therapy (ERT) with GLA is currently the most effective therapeutic strategy for patients with Fabry disease,a lysosomal storage disease.
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| Synonyms |
GLA, Agalsidase, Alpha-galactosidase A, Alpha-D-galactosidase A, Alpha-D-galactoside galactohydrolase, Galactosylgalactosylglucosylceramidase GLA
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| Swissprot | |
| Reactivity |
Human
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| Specificity |
Detects Human GLα in ELISAs
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| Applications |
ELISA
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| Storage |
-20℃
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| Expiration date |
12 months
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| Introduction |
This Antibody Pair Kit applies to the sandwich ELISA assay.
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