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GLA antibody (AA 80-429)

This anti-GLA antibody is a Mouse Monoclonal antibody detecting GLA in WB, IHC, ELISA and IF. Suitable for Human.
Catalog No. ABIN7114449

Quick Overview for GLA antibody (AA 80-429) (ABIN7114449)

Target

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

Reactivity

  • 86
  • 37
  • 27
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 94
  • 12
  • 2
Mouse

Clonality

  • 88
  • 20
Monoclonal

Conjugate

  • 52
  • 13
  • 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

  • 75
  • 32
  • 28
  • 26
  • 13
  • 13
  • 13
  • 12
  • 8
  • 6
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Clone

7F1
  • Binding Specificity

    • 16
    • 9
    • 7
    • 6
    • 5
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 80-429

    Purpose

    GLA antibody

    Purification

    Protein A+G purification

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    Immunogen sequence: 80-429aa

    Immunogen: galactosidase, alpha

    Isotype

    IgG2a
  • Application Notes

    WB: 1:500-1:2000, IHC: 1:20-1:200, IF: 1:20-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Storage Comment

    -20°C for 12 months

    Expiry Date

    12 months
  • Target

    GLA (Galactosidase, alpha (GLA))

    Alternative Name

    GLA

    Background

    Synonyms: Alpha-galactosidase A|Alpha-D-galactosidase A|Alpha-D-galactoside galactohydrolase|Galactosylgalactosylglucosylceramidase GLA|Melibiase|GLA

    Background: GLA, also named as Melibiase, Agalsidase and Alpha-galactosidase A, belongs to the glycosyl hydrolase 27 family. It hydrolyzes terminal, non-reducing alpha-D-galactose residues in alpha-D-galactosides, including galactose oligosaccharides, galactomannans and galactolipids. Fabry disease is an X-linked lysosomal storage disorder resulting from the deficient activity of GLA. Enzyme replacement therapy(ERT) with GLA is currently the most effective therapeutic strategy for patients with Fabry disease, a lysosomal storage disease.

    Molecular Weight

    49 kDa

    Gene ID

    2717

    UniProt

    P06280

    Pathways

    SARS-CoV-2 Protein Interactome
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