Galactosidase alpha Rabbit Monoclonal Antibody
Product Specifications
Background
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.
Product Name Alternative
Alpha gal A; GALA; Galactosidase; alpha; GLA; Melibiase
Gene Name
Galactosidase alpha
Gene ID
2717
Swiss Prot
P06280
Host
Rabbit
Reactivity
Human
Clonality
Monoclonal
Conjugation
Unconjugated
Applications
WB, IHC, IP
Purification
Affinity Purification
Dilution
WB 1:500-1:1000, IHC 1:50-1:100, IP 1:10-1:20
Form
Liquid
Buffer
Purified antibody in TBS with 0.05% sodium azide,0.05%BSA and 50% glycerol.
Modification
Unmodified
Molecular Weight
Calculated MW: 49 kDa; Observed MW: 49 kDa
Storage Conditions
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Isotype
IgG
Available Sizes
Frequently Asked Questions
More Discoveries
Explore Other Products
Browse additional items from our catalog
MBS7079862 Inquire
Recombinant Pseudendoclonium akinetum Cytochrome b6-f complex subunit 4 (petD), partial
Sign In for Pricing
View Details 
bsm-33308M-Cy7-01 20 µL
Actin, alpha skeletal muscle Monoclonal Antibody, Cy7 Conjugated
Sign In for Pricing
View Details bsm-33308M-Cy7-02 100 µL
Actin, alpha skeletal muscle Monoclonal Antibody, Cy7 Conjugated
Sign In for Pricing
View Details 