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EYA4 Antikörper (AA 28-205)

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch EYA4 in WB, ELISA, FACS und IHC (p). Es zeigt Reaktivität gegenüber Proben von Human, Ratte und Affe.
Produktnummer ABIN7873244
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für EYA4 Antikörper (AA 28-205) (ABIN7873244)

Target

Alle EYA4 Antikörper anzeigen
EYA4 (Eyes Absent Homolog 4 (EYA4))

Reaktivität

  • 42
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Ratte, Affe

Wirt

  • 41
  • 1
Kaninchen

Klonalität

  • 42
Polyklonal

Konjugat

  • 19
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser EYA4 Antikörper ist unkonjugiert

Applikation

  • 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))
  • Bindungsspezifität

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

    Verwendungszweck

    EYA4 Antibody

    Aufreinigung

    Affinity purified

    Immunogen

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

    Isotyp

    IgG
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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))

    Andere Bezeichnung

    EYA4

    Hintergrund

    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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