Positive control:
Lane 1: HepG2
Lane 2: 293T
Applications
-
WB
-
IHC-P
REACTIVITY
-
Human
-
Rat
SPECIFICATIONS
Product Type
Recombinant Rabbit monoclonal primary
Product Name
Recombinant GBA Monoclonal Antibody (ET1703-32)
Immunogen
Recombinant protein
Host
Rabbit
Positive Control
SK-Br-3 cell lysate, A549 cell lysate, MCF-7 cell lysate, human breast carcinoma tissue, human liver tissue, human pancreas tissue, human kidney tissue, rat liver tissue, rat kidney tissue, mouse pancreas tissue.
Conjugation
Unconjugated
Clonality
Monoclonal
Clone Number
JM10-76
PROPERTIES
Form
Liquid
Storage Condition
Store at +4C after thawing. Aliquot store at -20C or -80C. Avoid repeated freeze / thaw cycles.
Storage Buffer
1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration
1 ug/ul
PURIFICATION
Protein A affinity purified.
MOLECULAR WEIGHT
60 kDa
Isotype
IgG
APPLICATION DILUTION
-
WB
-
1:1,000-1:5,000
-
IHC-P
-
1:50-1:200
TARGET
UNIPROT #
PROTEIN NAME
GBA
SYNONYMS
Acid beta glucosidase antibody; Acid beta-glucosidase antibody; Alglucerase antibody; Beta glucocerebrosidase antibody; BETA GLUCOSIDASE, ACID antibody; Beta-glucocerebrosidase antibody; betaGC antibody; D glucosyl N acylsphingosine glucohydrolase antibody; D-glucosyl-N-acylsphingosine glucohydrolase antibody; EC 3.2.1.45 antibody; GBA antibody; Gba protein antibody; GBA1 antibody; GC antibody; GCase antibody; GCB antibody; GLCM_HUMAN antibody; GLUC antibody; Glucocerebrosidase (alt.) antibody; Glucocerebrosidase antibody; GLUCOCEREBROSIDASE PSEUDOGENE antibody; Glucosidase beta antibody; Glucosidase, beta, acid antibody; Glucosidase, beta; acid (includes glucosylceramidase) antibody; Glucosylceramidase antibody; Imiglucerase antibody; Lysosomal glucocerebrosidase antibody; OTTHUMP00000033992 antibody; OTTHUMP00000033993 antibody
SEQUENCE SIMILARITIES
Belongs to the glycosyl hydrolase 30 family.
SUBCELLULAR LOCATION
Lysosome membrane.
FUNCTION
β-Glucosidase is a predominantly liver enzyme which efficiently hydrolyzes β-D-glucoside and β-D-galactoside. Defects in β-glucosidase cause Gaucher disease, an inherited condition distinguished by the accumulation of glucosylceramide within the cells of the reticuloendothelial system. β-Glucosidase is used in enzyme replacement treatment aimed at treating Gaucher disease. The absorption of dietary flavonoid glycosides in humans involves a critical deglycosylation step that is mediated by epithelial β-glucosidases.