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EYA4 anticorps (AA 28-205)

Cet anticorps Lapin Polyclonal détecte spécifiquement EYA4 dans WB, ELISA, FACS et IHC (p). Il présente une réactivité avec des échantillons de Humain, Rat et Singe.
N° du produit ABIN7873244
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour EYA4 anticorps (AA 28-205) (ABIN7873244)

Antigène

Voir toutes EYA4 Anticorps
EYA4 (Eyes Absent Homolog 4 (EYA4))

Reactivité

  • 42
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain, Rat, Singe

Hôte

  • 41
  • 1
Lapin

Clonalité

  • 42
Polyclonal

Conjugué

  • 19
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp EYA4 est non-conjugé

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))
  • Épitope

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

    Fonction

    EYA4 Antibody

    Purification

    Affinity purified

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.
  • Antigène

    EYA4 (Eyes Absent Homolog 4 (EYA4))

    Autre désignation

    EYA4

    Sujet

    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
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