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PVRL4 Antikörper

Der Kaninchen Chimeric Anti-PVRL4 Antikörper wurde für FACS validiert. Er ist geeignet, PVRL4 in Proben von Human zu detektieren.
Produktnummer ABIN7490714

Kurzübersicht für PVRL4 Antikörper (ABIN7490714)

Target

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

Fragment

Fc fragment

Reaktivität

  • 54
  • 23
  • 13
Human

Wirt

  • 46
  • 6
  • 5
  • 2
Kaninchen

Klonalität

  • 47
  • 10
  • 1
Chimeric

Konjugat

  • 29
  • 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

  • 45
  • 28
  • 7
  • 4
  • 3
  • 3
  • 3
  • 1
Flow Cytometry (FACS)
  • Produktmerkmale

    Rabbit/Human Fc chimeric IgG1

    Aufreinigung

    Purified from cell culture supernatant by affinity chromatography

    Isotyp

    IgG1
  • Applikationshinweise

    Flow Cyt  1:100

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    Haltbarkeit

    12 months
  • Target

    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

    Andere Bezeichnung

    NECTIN4

    Hintergrund

    EDSS1, LNIR, nectin-4, PRR4, PVRL4,
    Description: 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.

    UniProt

    Q96NY8

    Pathways

    Cell-Cell Junction Organization
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