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GM2A antibody

GM2A Reactivity: Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7262481
  • Target See all GM2A Antibodies
    GM2A (GM2 Ganglioside Activator (GM2A))
    Reactivity
    • 59
    • 20
    • 19
    • 1
    • 1
    • 1
    • 1
    • 1
    Mouse, Rat
    Host
    • 52
    • 7
    • 2
    Rabbit
    Clonality
    • 56
    • 5
    Polyclonal
    Conjugate
    • 26
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This GM2A antibody is un-conjugated
    Application
    • 46
    • 27
    • 13
    • 13
    • 10
    • 6
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human GM2A (NP_000396.2).
    Isotype
    IgG
    Top Product
    Discover our top product GM2A Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 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
    GM2A (GM2 Ganglioside Activator (GM2A))
    Alternative Name
    GM2A (GM2A Products)
    Synonyms
    GM2A antibody, fb96e04 antibody, fb96e10 antibody, wu:fb96e04 antibody, wu:fb96e10 antibody, zgc:110188 antibody, MGC84154 antibody, GM2-AP antibody, SAP-3 antibody, AA408702 antibody, AW215435 antibody, GM2 ganglioside activator antibody, GM2 ganglioside activator L homeolog antibody, GM2 ganglioside activator protein antibody, Gm2a antibody, GM2A antibody, gm2a antibody, gm2a.L antibody
    Background
    This gene encodes a small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A. Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease. Alternative splicing results in multiple transcript variants.
    Molecular Weight

    Observed_MW: 26 kDa

    Calculated_MW: 20 kDa

    Gene ID
    2760
    UniProt
    P17900
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