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PVRL4 Antikörper

Dieses Anti-PVRL4-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von PVRL4 in WB, ELISA und IHC. Geeignet für Human und Maus.
Produktnummer ABIN7237516

Kurzübersicht für PVRL4 Antikörper (ABIN7237516)

Target

Alle PVRL4 Antikörper anzeigen
PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

Reaktivität

  • 57
  • 22
  • 13
Human, Maus

Wirt

  • 48
  • 6
  • 6
  • 2
Kaninchen

Klonalität

  • 48
  • 11
  • 2
Polyklonal

Konjugat

  • 32
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser PVRL4 Antikörper ist unkonjugiert

Applikation

  • 46
  • 29
  • 8
  • 5
  • 5
  • 5
  • 4
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant protein of human PVRL4

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:500-1:2000, IHC 1:100-1:300

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.9 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

    Andere Bezeichnung

    NECTIN4

    Hintergrund

    This gene encodes a member of the nectin family. The encoded protein contains two immunoglobulin-like (Ig-like) C2-type domains and one Ig-like V-type domain. It is involved in cell adhesion through trans-homophilic and -heterophilic interactions. It is a single-pass type I membrane protein. The soluble form is produced by proteolytic cleavage at the cell surface by the metalloproteinase ADAM17/TACE. The secreted form is found in both breast tumor cell lines and breast tumor patients. Mutations in this gene are the cause of ectodermal dysplasia-syndactyly syndrome type 1, an autosomal recessive disorder. Alternatively spliced transcript variants have been found but the full-length nature of the variant has not been determined.

    Molekulargewicht

    55 kDa

    UniProt

    Q96NY8

    Pathways

    Cell-Cell Junction Organization
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