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PVRL4 Antikörper (AA 53-94)

Der Kaninchen Polyklonal Anti-PVRL4-Antikörper wurde für WB validiert. Er ist geeignet, PVRL4 in Proben von Human zu detektieren.
Produktnummer ABIN5647906

Kurzübersicht für PVRL4 Antikörper (AA 53-94) (ABIN5647906)

Target

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

Reaktivität

  • 55
  • 23
  • 13
Human

Wirt

  • 47
  • 6
  • 5
  • 2
Kaninchen

Klonalität

  • 47
  • 10
  • 2
Polyklonal

Konjugat

  • 30
  • 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
  • 28
  • 8
  • 5
  • 4
  • 4
  • 3
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 7
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 53-94

    Aufreinigung

    Antigen affinity purified

    Immunogen

    Amino acids 53-94 (FYRGDSGEQVGQVAWARVDAGEGAQELALLHSKYGLHVSPAY) from the human protein were used as the immunogen for the Nectin-4 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Western blot: 0.5-1 μg/mL

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    -20 °C

    Informationen zur Lagerung

    After reconstitution, the Nectin-4 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

    Andere Bezeichnung

    Nectin-4 / PVRL4

    Hintergrund

    PVRL4, also known as Nectin-4, is expressed in human skin, hair follicles, and cultured keratinocytes, but not in fibroblasts. 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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