Anti-Galactosidase alpha Rabbit Monoclonal Antibody
Catalog No.
MA2740
Anti-Galactosidase alpha Rabbit Monoclonal Antibody
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Defects in GLA are the cause of Fabry disease (FD) [MIM:301500]. FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. The disease consists of an inborn error of glycosphingolipid catabolism.
2717
Alpha gal A; GALA; Galactosidase; alpha; GLA; Melibiase
Rabbit
Human
Unconjugated
Calculated MW: 49 kDa; Observed MW: 49 kDa
Unmodified
IgG
Monoclonal Antibody
AP-13F12B10
Liquid
See label
Carrier Not Free
A synthetic peptide of human Galactosidase alpha
Affinity Purified
50mM Tris-Glycine (pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA.
WB, IHC-P, IP
Blue ice
-20°C
12 months
Please avoid freeze-thaw cycles.