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PVRL4 antibody

The Rabbit Polyclonal anti-PVRL4 antibody (ABIN7237516) specifically detects PVRL4 in WB, ELISA and IHC. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN7237516
-15% Promotion 2026
$457.98
$538.80
save $80.82 (-15 %)
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for PVRL4 antibody (ABIN7237516)

Target

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

Reactivity

  • 75
  • 23
  • 14
Human, Mouse

Host

  • 48
  • 18
  • 12
  • 2
Rabbit

Clonality

  • 48
  • 29
  • 2
Polyclonal

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

  • 45
  • 28
  • 8
  • 5
  • 3
  • 3
  • 3
  • 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
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