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Invitrogen™ GBA Polyclonal Antibody
Rabbit Polyclonal Antibody
Marke: Invitrogen™ PA597773
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Beschreibung
GBA Polyclonal Antibody for Western Blot, IHC (P), ELISA
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 | |
| 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 | |
| Protein G | |
| RUO | |
| 2629 | |
| -20°C or -80°C if preferred | |
| Liquid |
| ELISA, Immunohistochemistry (Paraffin), Western Blot | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.03% ProClin 300; pH 7.4 | |
| P04062 | |
| GBA | |
| Recombinant Human Glucosylceramidase protein (215-343AA). | |
| 100 μg | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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