Anti-GBA Rabbit Monoclonal Antibody
Catalog No.
MA2771
Anti-GBA Rabbit Monoclonal Antibody
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Defects in GBA are the cause of Gaucher disease (GD) [MIM:230800]; also known as glucocerebrosidase deficiency. GD is the most prevalent lysosomal storage disease, characterized by accumulation of glucosylceramide in the reticulo-endothelial system.
2629
Alglucerase; betaGC; GBA1; GCase; GCB; GLUC; Glucosylceramidase; Imiglucerase
Rabbit
Human, Rat
Unconjugated
Calculated MW: 60 kDa; Observed MW: 60 kDa
Unmodified
IgG
Monoclonal Antibody
AP-17D12H8
Liquid
See label
Carrier Free
A synthesized peptide derived from human GBA
Affinity Chromatography
Rabbit IgG in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
WB, IHC-P
Blue ice
-20°C
12 months
Please avoid freeze-thaw cycles.