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Occludin Antikörper (AA 350-450)

This anti-Occludin antibody (ABIN6144995) is a Rabbit Polyclonal antibody detecting Occludin in WB. Suitable for Human.
Produktnummer ABIN6144995

Quick Overview for Occludin Antikörper (AA 350-450) (ABIN6144995)

Target

Alle Occludin (OCLN) Antikörper anzeigen
Occludin (OCLN)

Reaktivität

  • 107
  • 65
  • 45
  • 34
  • 18
  • 13
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
Human

Wirt

  • 95
  • 20
  • 3
  • 1
Kaninchen

Klonalität

  • 89
  • 30
Polyklonal

Konjugat

  • 60
  • 9
  • 6
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser Occludin Antikörper ist unkonjugiert

Applikation

  • 96
  • 37
  • 32
  • 27
  • 26
  • 26
  • 20
  • 18
  • 15
  • 13
  • 6
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 16
    • 16
    • 11
    • 9
    • 6
    • 6
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 350-450

    Sequenz

    VVQELPLTSP VDDFRQPRYS SGGNFETPSK RAPAKGRAGR SKRTEQDHYE TDYTTGGESC DELEEDWIRE YPPITSDQQR QLYKRNFDTG LQEYKSLQSE L

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 350-450 of human Occludin (NP_002529.1).

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Occludin (OCLN)

    Andere Bezeichnung

    OCLN

    Hintergrund

    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.,OCLN,BLCPMG,PPP1R115,PTORCH1,occludin,Occludin,Signal Transduction,Cell Biology & Developmental Biology,Apoptosis,Cell Adhesion,Tight Junctions,Cytoskeleton,OCLN

    Molekulargewicht

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

    Gen-ID

    100506658

    UniProt

    Q16625

    Pathways

    Cell-Cell Junction Organization, Hepatitis C
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