Human GBA Ready-To-Use IHC Kit
Catalog Number:
BSS-IHC0457H
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| Article Name: | Human GBA Ready-To-Use IHC Kit |
| Biozol Catalog Number: | BSS-IHC0457H |
| Supplier Catalog Number: | IHC0457H |
| Alternative Catalog Number: | BSS-IHC0457H-50 |
| Manufacturer: | Bioss |
| Category: | Kits/Assays |
| Species Reactivity: | Human |
| Alternative Names: | GBA, GC, GCase, Glucosidase beta, Acid beta glucosidase, Acid beta-glucosidase, Alglucerase, Beta glucocerebrosidase, BETA GLUCOSIDASE, ACID, Beta-glucocerebrosidase, betaGC,D glucosyl N acylsphingosine glucohydrolase, D-glucosyl-N-acylsphingosine glucohydrolase, EC 3.2.1.45 , Gba protein, GBA1, GC antibody GCase, GCB, GLCM_HUMAN, GLUC, Glucocerebrosidase (alt.), Glucocerebrosidase, GLUCOCEREBROSIDASE PSEUDOGENE, Glucosidase beta, Glucosidase, beta, acid, Glucosidase, beta, acid (includes glucosylceramidase), Glucosylceramidase, Imiglucerase, Lysosomal glucocerebrosidasea |
| 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 multipletranscript variants. |
| Samples: | FFPE tissue |
| Target: | Human GBA |

