GLB1 Mouse Monoclonal Antibody [Clone ID: LBI10B2]
Product Specifications
Background
This gene encodes beta-galactosidase-1, a lysosomal enzyme that hydrolyzes the terminal beta-galactose from ganglioside substrates and other glycoconjugates. Defects in this gene are the cause of GM1-gangliosidosis and Morquio B syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]
Synonyms
EBP; ELNR1; MPS4B
Gene Name
Homo sapiens galactosidase beta 1 (GLB1), transcript variant 2, mRNA.
Gene ID
2720
UniProt
P16278
Conjugation
Unconjugated
Related Pathways
Galactose metabolism, Glycosaminoglycan degradation, Glycosphingolipid biosynthesis - ganglio series, Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism
Field of Research
Galactose metabolism, Glycosaminoglycan degradation, Glycosphingolipid biosynthesis - ganglio series, Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism
Dilution
WB 1:200~2000, IF 1:100
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.
Symbol
GLB1
Overview
Carrier-free (BSA/glycerol-free) GLB1 mouse monoclonal antibody, clone LBI10B2
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=2720
Uniprot URL
https://www.uniprot.org/uniprot/P16278
Curated Selection
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