Human GBA Ready-To-Use IHC Kit
Artikelnummer:
BSS-IHC0457H
- Bilder (1)
| Artikelname: | Human GBA Ready-To-Use IHC Kit |
| Artikelnummer: | BSS-IHC0457H |
| Hersteller Artikelnummer: | IHC0457H |
| Alternativnummer: | BSS-IHC0457H-50 |
| Hersteller: | Bioss |
| Kategorie: | Kits/Assays |
| Spezies Reaktivität: | Human |
| Alternative Synonym: | 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. |
| Proben: | FFPE tissue |
| Target-Kategorie: | Human GBA |

