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TCTN2 Antikörper (PE)

TCTN2 Reaktivität: Human, Maus, Ratte WB Wirt: Kaninchen Polyclonal PE
Produktnummer ABIN1712697
  • Target Alle TCTN2 Antikörper anzeigen
    TCTN2 (Tectonic Family Member 2 (TCTN2))
    Reaktivität
    • 25
    • 14
    • 7
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 28
    • 1
    Kaninchen
    Klonalität
    • 28
    • 1
    Polyklonal
    Konjugat
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TCTN2 Antikörper ist konjugiert mit PE
    Applikation
    • 27
    • 13
    • 13
    • 8
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Kreuzreaktivität
    Maus
    Homologie
    Human,Rat
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human TCTN2
    Isotyp
    IgG
    Top Product
    Discover our top product TCTN2 Primärantikörper
  • Applikationshinweise
    FCM(1:20-100)
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Haltbarkeit
    12 months
  • Target
    TCTN2 (Tectonic Family Member 2 (TCTN2))
    Andere Bezeichnung
    Tctn2 (TCTN2 Produkte)
    Synonyme
    fb44f11 antikoerper, wu:fb44f11 antikoerper, tect2 antikoerper, C12orf38 antikoerper, MKS8 antikoerper, TECT2 antikoerper, 4432405B04Rik antikoerper, Tect2 antikoerper, tectonic family member 2 antikoerper, TCTN2 antikoerper, tctn2 antikoerper, Tctn2 antikoerper
    Hintergrund

    Synonyms: C12orf38, FLJ12975, MKS8, OTTHUMP00000239215, OTTHUMP00000239216, Tctn2, TECT2, TECT2_HUMAN, Tectonic family member 2, Tectonic-2.

    Background: Defects in TCTN2 are the cause of Meckel syndrome type 8 (MKS8) [MIM:613885]. A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly.

    Pathways
    Proton Transport
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