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Claudin 19 antibody

CLDN19 Reactivity: Human ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7190275
  • Target See all Claudin 19 (CLDN19) Antibodies
    Claudin 19 (CLDN19)
    Reactivity
    • 19
    • 18
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 31
    • 3
    Rabbit
    Clonality
    • 32
    • 2
    Polyclonal
    Conjugate
    • 13
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Claudin 19 antibody is un-conjugated
    Application
    • 13
    • 13
    • 12
    • 12
    • 3
    • 3
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Cross-Reactivity
    Human, Mouse, Rat
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of Human CLDN19
    Isotype
    IgG
    Top Product
    Discover our top product CLDN19 Primary Antibody
  • Application Notes
    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
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C,-80 °C
    Storage Comment
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target
    Claudin 19 (CLDN19)
    Alternative Name
    CLDN19 (CLDN19 Products)
    Synonyms
    HOMG5 antibody, claudin-19 antibody, zgc:112141 antibody, claudin 19 antibody, claudin 19 S homeolog antibody, CLDN19 antibody, Cldn19 antibody, cldn19.S antibody, cldn19 antibody
    Background

    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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