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Occludin antibody

OCLN Reactivity: Human, Mouse, Rat WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5964434
  • Target See all Occludin (OCLN) Antibodies
    Occludin (OCLN)
    Reactivity
    • 101
    • 64
    • 44
    • 34
    • 18
    • 11
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    Human, Mouse, Rat
    Host
    • 86
    • 17
    • 3
    • 1
    Rabbit
    Clonality
    • 85
    • 22
    Polyclonal
    Conjugate
    • 43
    • 10
    • 7
    • 6
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This Occludin antibody is un-conjugated
    Application
    • 85
    • 34
    • 28
    • 26
    • 26
    • 15
    • 15
    • 14
    • 11
    • 8
    • 7
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human Occludin (NP_002529.1).
    Isotype
    IgG
    Top Product
    Discover our top product OCLN Primary Antibody
  • Application Notes
    WB 1:500-1:2000 IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Occludin (OCLN)
    Alternative Name
    Occludin (OCLN Products)
    Synonyms
    AI503564 antibody, Ocl antibody, ocln antibody, oclnb antibody, tpmt antibody, OCLN antibody, wu:fd23h10 antibody, wu:fi13c01 antibody, zgc:113992 antibody, zgc:56359 antibody, BLCPMG antibody, occludin antibody, occludin S homeolog antibody, occludin a antibody, Ocln antibody, OCLN antibody, ocln.S antibody, ocln antibody, oclna antibody
    Background
    This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5.
    Molecular Weight

    Observed_MW: 68kDa

    Calculated_MW: 8kDa/23kDa/31kDa/52kDa/54kDa/59kDa

    Gene ID
    100506658
    UniProt
    Q16625
    Pathways
    Cell-Cell Junction Organization, Hepatitis C
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