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GLA antibody

GLA Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7267333
  • Target See all GLA Antibodies
    GLA (Galactosidase, alpha (GLA))
    Reactivity
    • 67
    • 33
    • 25
    • 4
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 79
    • 6
    • 2
    Rabbit
    Clonality
    • 80
    • 7
    Monoclonal
    Conjugate
    • 37
    • 12
    • 9
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GLA antibody is un-conjugated
    Application
    • 60
    • 33
    • 19
    • 15
    • 12
    • 12
    • 8
    • 8
    • 6
    • 6
    • 3
    • 3
    • 1
    Western Blotting (WB)
    Purpose
    Galactosidase alpha (GLA) Rabbit mAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human Galactosidase alpha (GLA) (GLA)
    Isotype
    IgG
    Top Product
    Discover our top product GLA Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    GLA (Galactosidase, alpha (GLA))
    Alternative Name
    GLA (GLA Products)
    Background
    This gene encodes 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. [provided by RefSeq, Jul 2008],GALA,Blood,Blood_Blood Cell Antigens,Cardiovascular,GLA
    Molecular Weight
    46kDa
    Gene ID
    2717
    UniProt
    P06280
    Pathways
    SARS-CoV-2 Protein Interactome
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