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GLB1 Antibody / 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.

Product Specifications

Specifications

Immunohistochemistry (FFPE) : 1:50

UniProt

P16278

Host

Rabbit

Reactivity

Human, Mouse, Rat

Immunogen

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

Clonality

Recombinant Monoclonal

Isotype

IgG

Clone

25G11

Applications

IHC-P

Purity

Affinity chromatography

Format

Purified

Limitations

This GLB1 antibody is available for research use only.

Storage Conditions

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.

Formulation

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

Applications Notes

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

Location

Cytoplasm

Image Legend

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.

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