GBA antibody [C1C3]

This gene 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 encoding the same protein. [provided by RefSeq]
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Reference:
GRP101
Brand:
Product Details
GRP101

Data sheet

Size
100 ul
Conjugation
Unconjugated
Host
Rabbit
Clonality
Polyclonal
Reactivity
Human
Application
ICC,IF,IHC-P,WB

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