GBA Mouse Monoclonal Antibody [Clone ID: LBI1D12]

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]

Overview

Carrier-free (BSA/glycerol-free) GBA mouse monoclonal antibody, clone LBI1D12

Synonyms

GBA1; GCB; GLUC

Gene Name

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

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

Dilution

WB 1:2000, IHC 1:150

Form

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

Buffer

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

Function

Druggable Genome

Storage Conditions

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.