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EYA4 antibody (AA 100-150)

This anti-EYA4 antibody is a Rabbit Polyclonal antibody detecting EYA4 in WB, IP and IHC (fp). Suitable for Human.
Catalog No. ABIN7453704

Quick Overview for EYA4 antibody (AA 100-150) (ABIN7453704)

Target

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

Reactivity

  • 40
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 39
  • 1
Rabbit

Clonality

  • 40
Polyclonal

Conjugate

  • 17
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EYA4 antibody is un-conjugated

Application

  • 18
  • 17
  • 13
  • 13
  • 13
  • 11
  • 7
  • 3
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 15
    • 9
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    AA 100-150

    Purpose

    Rabbit anti-EYA4 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 100 and 150

    Isotype

    IgG
  • Application Notes

    IHC: 1:100 - 1:500. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

    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

    4 °C

    Expiry Date

    12 months
  • Target

    EYA4 (Eyes Absent Homolog 4 (EYA4))

    Alternative Name

    EYA4

    Background

    Background: EYA4 (eyes absent homolog 4) is a member of the eyes absent (EYA) family of proteins. EYA4 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 the EYA4 gene are the cause of deafness utosomal dominant type 10 (DFNA10) and dilated cardiomyopathy 1J (CMD1J).

    Gene ID

    2070

    NCBI Accession

    NP_004091

    UniProt

    O95677

    Pathways

    Sensory Perception of Sound
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