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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

  • 57
  • 23
  • 13
Human

Wirt

  • 48
  • 6
  • 6
  • 2
Kaninchen

Klonalität

  • 49
  • 11
  • 1
Chimeric

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

  • 47
  • 30
  • 9
  • 5
  • 5
  • 4
  • 4
  • 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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