GBA

gene product
GBA1, GLUC
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]
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43 antibodies from 12 providers.

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AntibodyRefsTypeWBELIFIPIHFC
Novus Biologicals
9 antibodies
H00002629-M014Monoclonal
NBP1-32271Polyclonal
Abnova Corporation
6 antibodies
H00002629-M013Monoclonal
H00002629-D01Polyclonal
GeneTex
3 antibodies
GTX101267Polyclonal
GTX114073Polyclonal
Thermo Fisher Scientific Pierce
2 antibodies
PA5-21347Polyclonal
PA5-22326Polyclonal
Aviva Systems Biology
2 antibodies
OAAB05533Polyclonal
ARP61322_P050Polyclonal
Atlas Antibodies
1 antibody
HPA006667Polyclonal
Creative Biomart
5 antibodies
CAB-3392MHMonoclonal
CABT-10996MHMonoclonal
Epitomics
4 antibodies
3665-1Monoclonal
5719-1Monoclonal
antibodies-online
5 antibodies
ABIN401936Monoclonal
ABIN442242Polyclonal
Acris Antibodies GmbH
1 antibody
AP46301PU-NPolyclonal
LifeSpan BioSciences, Inc.
1 antibody
LS-C104954Monoclonal
Sigma-Aldrich
4 antibodies
WH0002629M1Monoclonal
HPA006667Polyclonal