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GLA antibody (C-Term)

This anti-GLA antibody is a Rabbit Polyclonal antibody detecting GLA in WB. Suitable for Mouse and Rat.
Catalog No. ABIN4886604

Quick Overview for GLA antibody (C-Term) (ABIN4886604)

Target

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

Reactivity

  • 100
  • 37
  • 26
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Mouse, Rat

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
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 218-275, C-Term

    Purpose

    Anti-Galactosidase alpha/Gla Antibody Picoband®

    Sequence

    DIQYYCNHWR NFDDVYDSWE SIKNILSWTV VYQKEIVEVA

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-Galactosidase alpha/Gla Antibody Picoband® (ABIN4886604). Tested in WB applications. This antibody reacts with Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    A synthetic peptide corresponding to a sequence at the C-terminus of mouse Gla, different from the related human sequence by fifteen amino acids.

    Isotype

    IgG
  • Application Notes

    Western blot, 0.1-0.5 μg/mL, Mouse, Rat
    1. "Entrez Gene: GLA galactosidase, alpha". 2. Calhoun DH, Bishop DF, Bernstein HS, Quinn M, Hantzopoulos P, Desnick RJ (1985). "Fabry disease: isolation of a cDNA clone encoding human alpha-galactosidase A". Proceedings of the National Academy of Sciences of the United States of America. 82 (21): 7364-8. 3. Keating GM (October 2012). "Agalsidase alfa: a review of its use in the management of Fabry disease". BioDrugs. 26 (5): 335-54.

    Comment

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Target

    GLA (Galactosidase, alpha (GLA))

    Alternative Name

    Gla

    Background

    Synonyms: Alpha-galactosidase A,3.2.1.22 ,Alpha-D-galactosidase A,Alpha-D-galactoside galactohydrolase,Melibiase,Gla,Ags,

    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.

    Molecular Weight

    49 kDa

    Gene ID

    11605

    UniProt

    P51569

    Pathways

    SARS-CoV-2 Protein Interactome
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