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

EYA4 antibody (AA 28-205)

This Rabbit Polyclonal antibody specifically detects EYA4 in WB, ELISA, FACS and IHC (p). It exhibits reactivity toward Human, Rat and Monkey.
Catalog No. ABIN7873244
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for EYA4 antibody (AA 28-205) (ABIN7873244)

Target

See all EYA4 Antibodies
EYA4 (Eyes Absent Homolog 4 (EYA4))

Reactivity

  • 42
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Rat, Monkey

Host

  • 41
  • 1
Rabbit

Clonality

  • 42
Polyclonal

Conjugate

  • 19
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EYA4 antibody is un-conjugated

Application

  • 20
  • 17
  • 14
  • 13
  • 13
  • 12
  • 7
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 15
    • 9
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    AA 28-205

    Purpose

    EYA4 Antibody

    Purification

    Affinity purified

    Immunogen

    Recombinant human protein (amino acids R28-E205) was used as the immunogen for the EYA4 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the EYA4 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the EYA4 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    EYA4 (Eyes Absent Homolog 4 (EYA4))

    Alternative Name

    EYA4

    Background

    This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant non-syndromic sensorineural 10 locus. The encoded protein is also a putative oncogene that mediates DNA repair, apoptosis, and innate immunity following DNA damage, cellular damage, and viral attack. Defects in this gene are also associated with dilated cardiomyopathy 1J. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    UniProt

    O95677

    Pathways

    Sensory Perception of Sound
You are here:
Chat with us!