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Tricellulin Antikörper

MARVELD2 Reaktivität: Human, Ratte, Maus WB, IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7120257
  • Target Alle Tricellulin (MARVELD2) Antikörper anzeigen
    Tricellulin (MARVELD2)
    Reaktivität
    • 32
    • 11
    • 10
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Ratte, Maus
    Wirt
    • 32
    Kaninchen
    Klonalität
    • 32
    Polyklonal
    Konjugat
    • 15
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser Tricellulin Antikörper ist unkonjugiert
    Applikation
    • 24
    • 14
    • 14
    • 3
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Aufreinigung
    Immunogen affinity purified
    Reinheit
    ≥95 % as determined by SDS-PAGE
    Immunogen
    MARVEL domain containing 2
    Isotyp
    IgG
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  • Applikationshinweise
    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    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.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    Haltbarkeit
    12 months
  • Target
    Tricellulin (MARVELD2)
    Andere Bezeichnung
    MARVELD2 (MARVELD2 Produkte)
    Synonyme
    Mrvldc2 antikoerper, BC003296 antikoerper, MARVD2 antikoerper, Tric antikoerper, Trica antikoerper, Tricb antikoerper, Tricc antikoerper, DFNB49 antikoerper, MRVLDC2 antikoerper, MARVEL domain containing 2 antikoerper, MARVEL (membrane-associating) domain containing 2 antikoerper, Marveld2 antikoerper, MARVELD2 antikoerper
    Hintergrund
    Synonyms:TRIC Background:The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene.
    Molekulargewicht
    69 kDa
    Gen-ID
    153562
    UniProt
    Q8N4S9
    Pathways
    Sensory Perception of Sound, Cell-Cell Junction Organization
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