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PVRL4 antibody (Biotin)

This Human Chimeric antibody specifically detects PVRL4 in FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7608322

Quick Overview for PVRL4 antibody (Biotin) (ABIN7608322)

Target

See all PVRL4 Antibodies
PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

Reactivity

  • 57
  • 23
  • 13
Human

Host

  • 48
  • 6
  • 5
  • 2
Human, Rabbit

Clonality

  • 49
  • 11
  • 1
Chimeric

Conjugate

  • 33
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PVRL4 antibody is conjugated to Biotin

Application

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

Clone

DMC438
  • Purpose

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

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG1
  • Application Notes

    Flow Cyt 1:100

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

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

    Storage

    -20 °C,-80 °C

    Storage Comment

    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.

    Expiry Date

    12 months
  • Target

    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

    Alternative Name

    NECTIN4

    Background

    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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