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PVRL4 Antikörper

Dieser 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

  • 53
  • 22
  • 13
Human, Maus

Wirt

  • 46
  • 5
  • 5
  • 2
Kaninchen

Klonalität

  • 46
  • 9
  • 2
Polyklonal

Konjugat

  • 28
  • 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

  • 44
  • 26
  • 6
  • 5
  • 3
  • 3
  • 3
  • 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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