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Occludin antibody

This Rabbit Polyclonal antibody specifically detects Occludin in WB, ELISA and IF. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN8123504
$225.50
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Occludin antibody (ABIN8123504)

Target

See all Occludin (OCLN) Antibodies
Occludin (OCLN)

Reactivity

  • 170
  • 85
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  • 14
  • 3
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  • 2
  • 2
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  • 2
Human, Mouse, Rat

Host

  • 154
  • 47
  • 4
  • 1
Rabbit

Clonality

  • 135
  • 71
Polyclonal

Conjugate

  • 91
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  • 5
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  • 4
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  • 4
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  • 3
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  • 3
  • 2
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  • 2
  • 2
  • 2
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  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
This Occludin antibody is un-conjugated

Application

  • 175
  • 76
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  • 16
  • 10
  • 3
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Western Blotting (WB), ELISA, Immunofluorescence (IF)
  • Purpose

    OCLN Antibody

    Specificity

    OCLN Polyclonal Antibody detects endogenous levels of protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogen

    Synthesized peptide derived from part region of human protein. AA350-400

    Isotype

    IgG
  • Application Notes

    WB 1:500-2000 IF 1:100-300 ELISA 1:5000-20000 Not yet tested in other applications.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

    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/1 year

    Expiry Date

    12 months
  • Target

    Occludin (OCLN)

    Alternative Name

    OCLN

    Background

    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. [provided by RefSeq, Apr 2011],

    Gene Name: OCLN

    Protein Name: Occludin, OCN

    Gene ID

    100506658

    UniProt

    Q16625

    Pathways

    Cell-Cell Junction Organization, Hepatitis C
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