GBA Mouse Monoclonal Antibody [Kloon ID: UMLBI171]

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. [provided by RefSeq, Jan 2010]

Carrier-free (BSA/glycerol-free) GBA mouse monoclonal antibody, clone UMLBI171

GBA1; GCB; GLUC

Homo sapiens glucosylceramidase beta (GBA), transcript variant 1, mRNA.

2629

P04062

Unconjugated

Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism

Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism

IHC 1:100~200

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

GBA

https://www.ncbi.nlm.nih.gov/gene/?term=2629

https://www.uniprot.org/uniprot/P04062