GBA Mouse Monoclonal Antibody [Clone ID: LBI4G4]
Product Specifications
Background
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]
Synonyms
GBA1; GCB; GLUC
Gene Name
Glucosylceramidase beta
Gene ID
2629
UniProt
P04062
Conjugation
Unconjugated
Related Pathways
Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism
Field of Research
Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism
Concentration
1 mg/ml
Dilution
WB 1:500, IHC 1:150
Form
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Buffer
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Function
Druggable Genome
Storage Conditions
Store 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.
Symbol
GBA
Overview
GBA mouse monoclonal antibody, clone LBI4G4
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=2629
Uniprot URL
https://www.uniprot.org/uniprot/P04062
Curated Selection
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