Galactosidase Alpha (GLA) Antibody

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Catalogue No: abx001425
Price: US$217.50
(Size: 20 µl)

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Galactosidase Alpha (GLA) Antibody Galactosidase Alpha (GLA) Antibody

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Datasheet SDS
GLA Antibody is a Rabbit Polyclonal antibody against GLA. 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.

Target Galactosidase Alpha (GLA)
Clonality Polyclonal
Reactivity Human, Mouse
Tested Applications ELISA, WB, IF/ICC
Host Rabbit
Recommended dilutions ELISA: 1 µg/ml, WB: 1/500 - 1/2000, IF/ICC: 1/50 - 1/100. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 150-429 of human Galactosidase alpha (GLA).
Isotype IgG
Form Liquid
Purification Purified by affinity chromatography.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC P06280 (UniProt, ExPASy)
UniProt Secondary AC Q6LER7
UniProt Entry Name AGAL_HUMAN
Gene Symbol GLA
GeneID 2717
NCBI Accession NP_000160.1
KEGG hsa:2717
String 9606.ENSP00000218516
Molecular Weight Calculated MW: 49 kDa
Observed MW: 49 kDa
Buffer PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Concentration > 0.2 mg/ml
Availability Shipped within 5-10 working days.
Note THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.
Research Articles on Galactosidase Alpha (GLA)


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