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Claudin 19 Antikörper

CLDN19 Reaktivität: Human ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7190275
  • Target Alle Claudin 19 (CLDN19) Antikörper anzeigen
    Claudin 19 (CLDN19)
    Reaktivität
    • 19
    • 18
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Wirt
    • 31
    • 3
    Kaninchen
    Klonalität
    • 32
    • 2
    Polyklonal
    Konjugat
    • 13
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser Claudin 19 Antikörper ist unkonjugiert
    Applikation
    • 13
    • 13
    • 12
    • 12
    • 3
    • 3
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Kreuzreaktivität
    Human, Maus, Ratte
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Synthetic peptide of Human CLDN19
    Isotyp
    IgG
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  • Applikationshinweise
    ELISA:1:2000-1:5000, IHC:1:25-1:100,
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % 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,-80 °C
    Informationen zur Lagerung
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target
    Claudin 19 (CLDN19)
    Andere Bezeichnung
    CLDN19 (CLDN19 Produkte)
    Synonyme
    HOMG5 antikoerper, claudin-19 antikoerper, zgc:112141 antikoerper, claudin 19 antikoerper, claudin 19 S homeolog antikoerper, CLDN19 antikoerper, Cldn19 antikoerper, cldn19.S antikoerper, cldn19 antikoerper
    Hintergrund

    Background: The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene.

    Aliases: CLDN19Claudin-19 antibody

    UniProt
    Q8N6F1
    Pathways
    Cell-Cell Junction Organization, Hepatitis C
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