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PVRL4 Antikörper (Biotin)

Dieses Human Chimeric-Antikörper erkennt spezifisch PVRL4 in FACS. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7608322

Kurzübersicht für PVRL4 Antikörper (Biotin) (ABIN7608322)

Target

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

Reaktivität

  • 57
  • 23
  • 13
Human

Wirt

  • 48
  • 6
  • 5
  • 2
Human, Kaninchen

Klonalität

  • 49
  • 11
  • 1
Chimeric

Konjugat

  • 33
  • 3
  • 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 konjugiert mit Biotin

Applikation

  • 47
  • 30
  • 9
  • 5
  • 5
  • 4
  • 4
  • 1
Flow Cytometry (FACS)

Klon

DMC438
  • Verwendungszweck

    Biotinylated Anti-Nectin4 antibody(DMC438), IgG1 Chimeric mAb

    Aufreinigung

    Purified from cell culture supernatant by affinity chromatography

    Isotyp

    IgG1
  • Applikationshinweise

    Flow Cyt 1:100

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    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

    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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