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Claudin 19 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement Claudin 19 dans ELISA et IHC. Il présente une réactivité envers Humain.
N° du produit ABIN7190275

Aperçu rapide pour Claudin 19 anticorps (ABIN7190275)

Antigène

Voir toutes Claudin 19 (CLDN19) Anticorps
Claudin 19 (CLDN19)

Reactivité

  • 18
  • 18
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Humain

Hôte

  • 30
  • 3
Lapin

Clonalité

  • 31
  • 2
Polyclonal

Conjugué

  • 12
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Claudin 19 est non-conjugé

Application

  • 13
  • 13
  • 11
  • 11
  • 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
  • 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

    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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