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GBA Mouse anti-Human, Clone: OTI4G4, lyophilized, TrueMAB™

Mouse Monoclonal Antibody
Supplier: OriGene CF803377

Description
Reconstitute with PBS (pH 7.3) and recommend to perform another round of desalting process using Product No. 7KMWCO
GBA 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.Specifications
GBA | |
Monoclonal | |
Unconjugated | |
GBA | |
GBA1, GCB, GLUC | |
Mouse | |
Affinity Chromatography | |
RUO | |
2629 | |
-20° C, Avoid Freeze/Thaw Cycles | |
Lyophilized |
Immunohistochemistry (Paraffin), Western Blot | |
OTI4G4 | |
PBS with 8% trehalose and no preservative; pH 7.3 | |
P04062 | |
GBA | |
Human recombit protein fragment corresponding to amino acids 40-315 of human GBA produced in E.coli. | |
100 μg | |
Primary | |
Human | |
Antibody | |
IgG2a |
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