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Invitrogen™ GBA Recombinant Rabbit Monoclonal Antibody (23GB5775), Invitrogen™
Rabbit Recombinant Monoclonal Antibody
Marke: Invitrogen™ MA552914
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Beschreibung
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.
Spezifikation
| GBA | |
| Recombinant Monoclonal | |
| 0.25 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
| P04062, P17439 | |
| GBA | |
| A synthesized peptide derived from human GBA (497-536AA). | |
| 100 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
| Flow Cytometry, Western Blot, Immunocytochemistry | |
| 23GB5775 | |
| 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 | |
| Affinity chromatography | |
| RUO | |
| 14466, 2629, 684536 | |
| -20°C | |
| Liquid |
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