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PVRL4 antibody (Biotin)

This Human Chimeric antibody specifically detects PVRL4 in FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7608322
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$223.29
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10 μg
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Quick Overview for PVRL4 antibody (Biotin) (ABIN7608322)

Target

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

Reactivity

  • 75
  • 24
  • 14
Human

Host

  • 48
  • 17
  • 12
  • 2
Human, Rabbit

Clonality

  • 49
  • 29
  • 1
Chimeric

Conjugate

  • 39
  • 6
  • 4
  • 4
  • 3
  • 3
  • 3
  • 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

  • 46
  • 29
  • 9
  • 4
  • 3
  • 3
  • 3
  • 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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