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Glucosidase, beta Antikörper (AA 65-354)

Reaktivität: Human WB, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN1886602
  • Target Alle Glucosidase, beta Produkte
    Glucosidase, beta
    Bindungsspezifität
    AA 65-354
    Reaktivität
    • 6
    • 2
    • 1
    Human
    Wirt
    • 9
    Kaninchen
    Klonalität
    • 9
    Polyklonal
    Konjugat
    • 5
    • 4
    Dieser Glucosidase, beta Antikörper ist unkonjugiert
    Applikation
    • 9
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (IHC)
    Aufreinigung
    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
  • Applikationshinweise
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.500
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    Konservierungsmittel
    Thimerosal (Merthiolate)
    Vorsichtsmaßnahmen
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target
    Glucosidase, beta
    Andere Bezeichnung
    beta-glucosidase (Glucosidase, beta Produkte)
    Synonyme
    BETA-GLUCOSIDASE antikoerper, GLUC antikoerper, T12J13.8 antikoerper, T12J13_8 antikoerper, beta glucosidase 25 antikoerper, PSPTO3318 antikoerper, PSPTO4290 antikoerper, beta glucosidase 25 antikoerper, beta-glucosidase antikoerper, Beta-glucosidase antikoerper, glucosylceramidase antikoerper, bglX-2 antikoerper, BGLU25 antikoerper, PSPTO_3318 antikoerper, bglX antikoerper, bglA4 antikoerper, LOC100399524 antikoerper, bglA.2 antikoerper, bglX-2 antikoerper
    Hintergrund
    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]
    Molekulargewicht
    60 kDa
    Gen-ID
    2629
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