Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

PVRL4 antibody

The Rabbit Chimeric anti-PVRL4 antibody is suitable to detect PVRL4 in samples from Human. It has been validated for FACS.
Catalog No. ABIN7490714
-15% Promotion 2026
$560.53
$659.45
save $98.92 (-15 %)
Plus shipping costs $50.00
Shipping to: United States
Delivery in 12 to 14 Business Days

Quick Overview for PVRL4 antibody (ABIN7490714)

Target

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

Fragment

Fc fragment

Reactivity

  • 75
  • 24
  • 14
Human

Host

  • 48
  • 18
  • 12
  • 2
Rabbit

Clonality

  • 49
  • 29
  • 1
Chimeric

Conjugate

  • 38
  • 6
  • 4
  • 4
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PVRL4 antibody is un-conjugated

Application

  • 46
  • 29
  • 9
  • 4
  • 3
  • 3
  • 3
  • 1
Flow Cytometry (FACS)
  • Characteristics

    Rabbit/Human Fc chimeric IgG1

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG1
  • Application Notes

    Flow Cyt  1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    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
You are here:
Chat with us!