Human GBA Ready-To-Use IHC Kit

Bioss

Human GBA Ready-To-Use IHC Kit

16

ImmunoHistoChemistry

Research Use Only

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.

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