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Invitrogen™ GBA Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA567940
Description
Predicted to react with Mouse samples.
GBA encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.
Specifications
GBA | |
Polyclonal | |
Unconjugated | |
GBA | |
acid beta glucosidase; acid beta-glucosidase; Alglucerase; betaGC; beta-GC; Beta-glucocerebrosidase; Cholesterol glucosyltransferase; Cholesteryl-beta-glucosidase; D-glucosyl-N-acylsphingosine glucohydrolase; Gba; GBA1; GBAP; GBAP1; GC; GCase; GCB; GLUC; glucocerebrosidase; glucosidase, beta, acid; glucosylceramidase; glucosylceramidase beta; glucosylceramidase beta pseudogene 1; glucosylceramidase-like protein; imiglucerase; Lysosomal acid GCase; Lysosomal acid glucosylceramidase; lysosomal glucocerebrosidase; SGTase | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
14466, 2629 | |
-20°C | |
Liquid |
Western Blot, Immunocytochemistry | |
1.0 mg/mL | |
PBS with 40% glycerol and 0.05% sodium azide; pH 7.4 | |
P04062, P17439 | |
GBA | |
Synthesized peptide derived from human GBA. | |
100 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
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