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Hexosaminidase A Antikörper

HEXA Reaktivität: Human WB, FACS, EIA Wirt: Maus Monoclonal 3F10 unconjugated
Produktnummer ABIN1105521
  • Target Alle Hexosaminidase A (HEXA) Antikörper anzeigen
    Hexosaminidase A (HEXA)
    Reaktivität
    • 57
    • 25
    • 14
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 48
    • 13
    Maus
    Klonalität
    • 50
    • 11
    Monoklonal
    Konjugat
    • 40
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser Hexosaminidase A Antikörper ist unkonjugiert
    Applikation
    • 48
    • 30
    • 14
    • 9
    • 6
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), Flow Cytometry (FACS), Enzyme Immunoassay (EIA)
    Spezifität
    Recognizes Beta-hexosaminidase alpha / HEXA
    Kreuzreaktivität (Details)
    Species reactivity (tested):Human.
    Aufreinigung
    Purified
    Klon
    3F10
    Isotyp
    IgG2b
    Top Product
    Discover our top product HEXA Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.0 mg/mL
    Buffer
    PBS, 0.05 % Sodium Azide, 0.5 % protein stabilizer
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Target
    Hexosaminidase A (HEXA)
    Andere Bezeichnung
    beta-Hexosaminidase alpha / HEXA (HEXA Produkte)
    Hintergrund
    This gene encodes the alpha subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Alpha subunit gene mutations lead to Tay-Sachs disease (GM2-gangliosidosis type I).Synonyms: Beta-N-acetylhexosaminidase subunit alpha, N-acetyl-beta-glucosaminidase subunit alpha
    Molekulargewicht
    60.7 kDa
    Gen-ID
    3073
    Pathways
    Sensory Perception of Sound, Glycosaminoglycan Metabolic Process
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