- Tel: 858.663.9055
-
Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
GLB1 (Beta-galactosidase) is a lysosomal hydrolase that catalyzes the breakdown of terminal beta-galactosides into monosaccharides. This enzyme is critical for the proper degradation of glycolipids, glycoproteins, and glycosaminoglycans. Researchers commonly use a GLB1 antibody to study lysosomal function and carbohydrate metabolism.
Deficiency of GLB1 activity is associated with lysosomal storage disorders such as GM1 gangliosidosis and Morquio B disease. These conditions highlight the importance of GLB1 in cellular homeostasis and human health. Employing a GLB1 antibody enables detection of protein expression and activity in both normal physiology and disease contexts.
NSJ Bioreagents provides a high-quality GLB1 antibody validated for applications including western blot, immunohistochemistry, and immunofluorescence. Using a GLB1 antibody ensures sensitive and reproducible results for studies of lysosomal biology, enzymatic function, and inherited metabolic disorders.
Optimal dilution of the GLB1 antibody should be determined by the researcher.
A peptide sequence specific to Beta galactosidase protein was used as the immunogen for the GLB1 antibody.
After reconstitution, the GLB1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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