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GLA antibody (AA 218-275)

This anti-GLA antibody is a Rabbit Polyclonal antibody detecting GLA in WB. Suitable for Mouse.
Catalog No. ABIN5647751

Quick Overview for GLA antibody (AA 218-275) (ABIN5647751)

Target

See all GLA Antibodies
GLA (Galactosidase, alpha (GLA))

Reactivity

  • 100
  • 37
  • 27
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Mouse

Host

  • 102
  • 18
  • 2
Rabbit

Clonality

  • 94
  • 28
Polyclonal

Conjugate

  • 64
  • 15
  • 13
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GLA antibody is un-conjugated

Application

  • 86
  • 40
  • 35
  • 30
  • 21
  • 19
  • 13
  • 13
  • 10
  • 6
  • 4
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 16
    • 12
    • 8
    • 7
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 218-275

    Purification

    Antigen affinity purified

    Immunogen

    Amino acids 218-275 (DIQYYCNHWRNFDDVYDSWESIKNILSWTVVYQKEIVEVA-mouse) were used as the immunogen for the Gla antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Gla antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    -20 °C

    Storage Comment

    After reconstitution, the Gla 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.
  • Target

    GLA (Galactosidase, alpha (GLA))

    Alternative Name

    Gla / Galactosidase alpha

    Background

    Alpha-galactosidase is a glycoside hydrolase enzyme that encoded by the GLA gene. This gene is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.

    UniProt

    P51569

    Pathways

    SARS-CoV-2 Protein Interactome
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