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TMEM67 Antikörper

TMEM67 Reaktivität: Maus, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN6293383
  • Target Alle TMEM67 Antikörper anzeigen
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Reaktivität
    Maus, Ratte
    Wirt
    • 19
    Kaninchen
    Klonalität
    • 19
    Polyklonal
    Konjugat
    • 9
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TMEM67 Antikörper ist unkonjugiert
    Applikation
    • 7
    • 6
    • 4
    • 2
    Western Blotting (WB)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein of human TMEM67
    Isotyp
    IgG
    Top Product
    Discover our top product TMEM67 Primärantikörper
  • Applikationshinweise
    WB 1:200 - 1:2000
    Kommentare

    Widely expressed in adult and fetal tissues, Expressed at higher level in spinal cord

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • 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 -20C. Avoid freeze / thaw cycles.
  • Target
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Andere Bezeichnung
    TMEM67 (TMEM67 Produkte)
    Synonyme
    JBTS6 antikoerper, MECKELIN antikoerper, MKS3 antikoerper, NPHP11 antikoerper, TNEM67 antikoerper, 5330408M12Rik antikoerper, B230117O07 antikoerper, b2b1163.1Clo antikoerper, b2b1291.1Clo antikoerper, Wpk antikoerper, transmembrane protein 67 antikoerper, TMEM67 antikoerper, tmem67 antikoerper, Tmem67 antikoerper
    Hintergrund
    The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).
    Molekulargewicht
    111.745 kDa
    Gen-ID
    91147
    UniProt
    Q5HYA8
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