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

PVRL4 antibody

This anti-PVRL4 antibody is a Rabbit Polyclonal antibody detecting PVRL4 in WB, ELISA and IHC. Suitable for Human and Mouse.
Catalog No. ABIN7237516

Quick Overview for PVRL4 antibody (ABIN7237516)

Target

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

Reactivity

  • 57
  • 22
  • 13
Human, Mouse

Host

  • 48
  • 6
  • 6
  • 2
Rabbit

Clonality

  • 48
  • 11
  • 2
Polyclonal

Conjugate

  • 32
  • 4
  • 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 un-conjugated

Application

  • 46
  • 29
  • 8
  • 5
  • 5
  • 5
  • 4
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human PVRL4

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:100-1:300

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.9 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • 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.

    Molecular Weight

    55 kDa

    UniProt

    Q96NY8

    Pathways

    Cell-Cell Junction Organization
You are here:
Chat with us!