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Beta Galactosidase Antibody

Beta-galactosidase: An essential enzyme

Overview

Beta-galactosidase, also known as beta-Gal or GLB1, is an essential enzyme that hydrolyzes beta-galactosides into monosaccharides. It cleaves beta-linked terminal galactosyl residues from gangliosides, glycoproteins, and glycosaminoglycans.

Antibody Type Catalog number Applications Citations
Beta-galactosidase Rabbit polyclonal 15518-1-AP ELISA, WB, IF, IHC 6
View the Beta-galactosidase product page here
 Beta Galactosidase  
Immunofluorescent analysis of Hela cells using GLB1 antibody at 1.25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red) SH-SY5Y cells were subjected to SDS PAGE followed by western blot with 15518-1-AP(GLB1 antibody) at dilution of 1:400
Immunofluorescent analysis of Hela cells using GLB1 antibody at 1.25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red). SH-SY5Y cells were subjected to SDS PAGE followed by western blot with 15518-1-AP(GLB1 antibody) at dilution of 1:400
Immunohistochemical analysis of paraffin-embedded human liver cancer tissue slide using 15518-1-AP (Beta galactosidase Antibody) Immunofluorescent analysis of fixed HeLa cells using Beta Galactosidase antibody (15518-1-AP) and CoraLite®488-Conjugated IgG(H+L), CL594-Phalloidin (red).
Immunohistochemical analysis of paraffin-embedded human liver cancer tissue slide using 15518-1-AP (Beta galactosidase Antibody) at dilution of 1:50 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). Immunofluorescent analysis of (-20°C Ethanol) fixed HeLa cells using Beta Galactosidase antibody (15518-1-AP) at dilution of 1:200 and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L), CL594-Phalloidin (red).

GLB1 (Beta-galactosidase) is also named as ELNR1, Lactase. It cleaves beta-linked terminal galactosyl residues from gangliosides, glycoproteins, and glycosaminoglycans. This protein is identical to the elastin-binding protein (EBP), a major component of the nonintegrin cell surface receptor complex expressed in fibroblasts, smooth muscle cells, chondroblasts, leukocytes, and certain cancer cell types. Defects in GLB1 are the cause of GM1-gangliosidosis type 1 (GM1G1), GM1-gangliosidosis type 2 (GM1G2), GM1-gangliosidosis type 3 (GM1G3) and mucopolysaccharidosis type 4B (MPS4B).

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