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SGSH Antikörper

SGSH Reaktivität: Human, Ratte, Maus WB, IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5700039
  • Target Alle SGSH Antikörper anzeigen
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    Reaktivität
    • 32
    • 19
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Ratte, Maus
    Wirt
    • 44
    • 3
    • 1
    Kaninchen
    Klonalität
    • 47
    • 1
    Polyklonal
    Konjugat
    • 23
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser SGSH Antikörper ist unkonjugiert
    Applikation
    • 46
    • 17
    • 13
    • 13
    • 7
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Immunogen
    N-sulfoglucosamine sulfohydrolase
    Isotyp
    IgG
    Top Product
    Discover our top product SGSH Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Kommentare

    HEK-293 cells were subjected to SDS PAGE followed by western blot with FNab07813( SGSH Antibody) at dilution of 1:600

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handhabung
    Avoid repeated freeze / thaw cycles.
    Lagerung
    -20 °C
    Haltbarkeit
    12 months
  • Target
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    Andere Bezeichnung
    SGSH (SGSH Produkte)
    Synonyme
    HSS antikoerper, MPS3A antikoerper, SFMD antikoerper, 4632406A19Rik antikoerper, N-sulfoglucosamine sulfohydrolase antikoerper, N-sulfoglucosamine sulfohydrolase (sulfamidase) antikoerper, SGSH antikoerper, Sgsh antikoerper
    Hintergrund
    Synonyms:HSS Background:This gene encodes one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.
    Gen-ID
    6448
    UniProt
    P51688
    Pathways
    Glycosaminoglycan Metabolic Process
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