GLB1 Antilichaam / Beta galactosidase

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.

Immunohistochemistry (FFPE) : 1:50

P16278

Human, Mouse, Rat

A peptide sequence specific to Beta galactosidase protein was used as the immunogen for the GLB1 antibody.

25G11

IHC-P

Affinity chromatography

Purified

This GLB1 antibody is available for research use only.

After reconstitution, the GLB1 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Antibody in PBS with 0.02% sodium azide, 50% glycerol and 0.4-0.5 mg/mL BSA

Optimal dilution of the GLB1 antibody should be determined by the researcher.

Cytoplasm

IHC staining of FFPE rat kidney tissue with GLB1 antibody, HRP-secondary and DAB substrate. HIER: boil tissue sections in pH8 EDTA for 20 min and allow to cool before testing.