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Claudin 19 anticorps

CLDN19 Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7190275
  • Antigène Voir toutes Claudin 19 (CLDN19) Anticorps
    Claudin 19 (CLDN19)
    Reactivité
    • 20
    • 19
    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Humain
    Hôte
    • 32
    • 3
    Lapin
    Clonalité
    • 33
    • 2
    Polyclonal
    Conjugué
    • 14
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Claudin 19 est non-conjugé
    Application
    • 13
    • 13
    • 13
    • 12
    • 3
    • 3
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
     Réactivité croisée
    Humain, Souris, Rat
    Purification
    Antigen affinity purification
    Immunogène
    Synthetic peptide of Human CLDN19
    Isotype
    IgG
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    Discover our top product CLDN19 Anticorps primaire
  • Indications d'application
    ELISA:1:2000-1:5000, IHC:1:25-1:100,
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C,-80 °C
    Stockage commentaire
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Antigène
    Claudin 19 (CLDN19)
    Autre désignation
    CLDN19 (CLDN19 Produits)
    Synonymes
    anticorps HOMG5, anticorps claudin-19, anticorps zgc:112141, anticorps claudin 19, anticorps claudin 19 S homeolog, anticorps CLDN19, anticorps Cldn19, anticorps cldn19.S, anticorps cldn19
    Sujet

    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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