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B9D1 Antikörper

B9D1 Reaktivität: Human, Maus, Ratte IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7264023
  • Target Alle B9D1 Antikörper anzeigen
    B9D1 (B9 Protein Domain 1 (B9D1))
    Reaktivität
    • 9
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 8
    • 1
    Kaninchen
    Klonalität
    • 9
    Polyklonal
    Konjugat
    • 9
    Dieser B9D1 Antikörper ist unkonjugiert
    Applikation
    • 9
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human B9D1 (NP_056496.1).
    Isotyp
    IgG
    Top Product
    Discover our top product B9D1 Primärantikörper
  • Applikationshinweise
    IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 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.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    B9D1 (B9 Protein Domain 1 (B9D1))
    Andere Bezeichnung
    B9D1 (B9D1 Produkte)
    Synonyme
    B9 antikoerper, EPPB9 antikoerper, MKS9 antikoerper, MKSR1 antikoerper, AW045994 antikoerper, Eppb9 antikoerper, im:6905750 antikoerper, im:7069491 antikoerper, wu:fc09g07 antikoerper, zgc:110733 antikoerper, B9 domain containing 1 antikoerper, B9 protein domain 1 antikoerper, B9D1 antikoerper, B9d1 antikoerper, b9d1 antikoerper
    Hintergrund
    This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17.
    Gen-ID
    27077
    UniProt
    Q9UPM9
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