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Glucosidase, beta antibody (AA 65-354)

Reactivity: Human WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1886602
  • Target See all Glucosidase, beta products
    Glucosidase, beta
    Binding Specificity
    AA 65-354
    Reactivity
    • 6
    • 2
    • 1
    Human
    Host
    • 9
    Rabbit
    Clonality
    • 9
    Polyclonal
    Conjugate
    • 5
    • 4
    This Glucosidase, beta antibody is un-conjugated
    Application
    • 9
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purification
    Purified by antigen-affinity chromatography.
    Immunogen
    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 65 and 354 of beta-glucosidase
  • Application Notes
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.500
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    Preservative
    Thimerosal (Merthiolate)
    Precaution of Use
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target
    Glucosidase, beta
    Alternative Name
    beta-glucosidase (Glucosidase, beta Products)
    Synonyms
    BETA-GLUCOSIDASE antibody, GLUC antibody, T12J13.8 antibody, T12J13_8 antibody, beta glucosidase 25 antibody, PSPTO3318 antibody, PSPTO4290 antibody, beta glucosidase 25 antibody, beta-glucosidase antibody, Beta-glucosidase antibody, glucosylceramidase antibody, bglX-2 antibody, BGLU25 antibody, PSPTO_3318 antibody, bglX antibody, bglA4 antibody, LOC100399524 antibody, bglA.2 antibody, bglX-2 antibody
    Background
    This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism.Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides.A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1.Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq]
    Molecular Weight
    60 kDa
    Gene ID
    2629
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