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beta-Galactosidase-1/GLB1 Products

beta-Galactosidase-1 (GLB1) is a lysosomal beta-galactosidase that hydrolyzes the terminal beta-galactose from ganglioside and keratan sulfate. Defects in this gene are the causes of lysosomal storage diseases for GM1-gangliosidosis and Morquio B syndrome (also known as mucopolysaccharidosis IVB). In GM1 gangliosidosis, GM1 ganglioside accumulates in the neurons of the central nervous system, because of the deficiency (0 plus or minus 3% of normal) of lysosomal beta-galactosidase activity. GM1 gangliosidosis demonstrates varying degrees of clinical severity but is invariably fatal, and children with the most common and severe form of GM1 gangliosidosis usually die within 3 years of birth. Morquio B syndrome patients are neurologically normal, but display severe skeletal dysostosis multiplex because of an accumulation of keratan sulfate. More than 100 mutations have been identified for GLB1, which result in different residual activities of the mutant enzymes and a spectrum of symptoms in the two related diseases. In lysosome, the mature beta-galactosidase protein associates with cathepsin A and neuraminidase 1 to form the lysosomal multienzyme complex. An alternative splicing at the RNA level of GLB1 results a catalytically inactive beta-galactosidase (also called elastin-binding protein) that plays an important role in vascular development.

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45 results for "beta-Galactosidase-1/GLB1" in Products

45 results for "beta-Galactosidase-1/GLB1" in Products

beta-Galactosidase-1/GLB1 Products

beta-Galactosidase-1 (GLB1) is a lysosomal beta-galactosidase that hydrolyzes the terminal beta-galactose from ganglioside and keratan sulfate. Defects in this gene are the causes of lysosomal storage diseases for GM1-gangliosidosis and Morquio B syndrome (also known as mucopolysaccharidosis IVB). In GM1 gangliosidosis, GM1 ganglioside accumulates in the neurons of the central nervous system, because of the deficiency (0 plus or minus 3% of normal) of lysosomal beta-galactosidase activity. GM1 gangliosidosis demonstrates varying degrees of clinical severity but is invariably fatal, and children with the most common and severe form of GM1 gangliosidosis usually die within 3 years of birth. Morquio B syndrome patients are neurologically normal, but display severe skeletal dysostosis multiplex because of an accumulation of keratan sulfate. More than 100 mutations have been identified for GLB1, which result in different residual activities of the mutant enzymes and a spectrum of symptoms in the two related diseases. In lysosome, the mature beta-galactosidase protein associates with cathepsin A and neuraminidase 1 to form the lysosomal multienzyme complex. An alternative splicing at the RNA level of GLB1 results a catalytically inactive beta-galactosidase (also called elastin-binding protein) that plays an important role in vascular development.

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Applications: ELISA
Applications: IHC, WB, ICC/IF
Reactivity: Human, Mouse, Canine, Monkey, Non-species specific
Applications: WB, Simple Western
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB, Flow
Reactivity: Human, Mouse, Rat

Recombinant Monoclonal Antibody

Applications: IHC
Reactivity: Human
Applications: WB, ELISA, IP
Reactivity: Human
Applications: IHC, WB, ICC/IF
Reactivity: Human, Rat
Applications: WB
Reactivity: Mouse, Rat
Applications: WB
Reactivity: Human, Mouse, Rat

Recombinant Monoclonal Antibody

Applications: WB
Applications: ICC/IF
Reactivity: Human
Applications: ELISA
Applications: AC
Applications: AC
Applications: IHC, WB
Reactivity: Human, Canine, Monkey
Applications: IHC, WB
Reactivity: Human, Canine, Monkey
Applications: IHC, WB
Reactivity: Human, Canine, Monkey
Applications: IHC, WB
Reactivity: Human, Canine, Monkey
Applications: IHC, WB
Reactivity: Human, Canine, Monkey
Applications: IHC
Reactivity: Human, Canine, Monkey
Applications: IHC
Reactivity: Human, Canine, Monkey
Applications: IHC
Reactivity: Human, Canine, Monkey
Applications: IHC
Reactivity: Human, Canine, Monkey
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