GLB1 Antibody / Beta galactosidase

• Description:

  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.

• 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.