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EYA1 antibody (N-Term)

This anti-EYA1 antibody is a Rabbit Polyclonal antibody detecting EYA1 in WB and EIA. Suitable for Human and Mouse.
Catalog No. ABIN952149

Quick Overview for EYA1 antibody (N-Term) (ABIN952149)

Target

See all EYA1 Antibodies
EYA1 (Eyes Absent Homolog 1 (EYA1))

Reactivity

  • 34
  • 18
  • 8
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
Human, Mouse

Host

  • 39
  • 1
  • 1
Rabbit

Clonality

  • 41
Polyclonal

Conjugate

  • 18
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EYA1 antibody is un-conjugated

Application

  • 21
  • 18
  • 13
  • 13
  • 4
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 15
    • 9
    • 5
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-30, N-Term

    Specificity

    This antibody recognizes Mouse EYA1 (N-term).

    Purification

    Affinity Chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human EYA1.

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    EYA1 (Eyes Absent Homolog 1 (EYA1))

    Alternative Name

    EYA1

    Background

    This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Four transcript variants encoding three distinct isoforms have been identified for this gene.Synonyms: Eyes absent homolog 1

    Molecular Weight

    64593 Da

    Gene ID

    2138

    NCBI Accession

    NP_000494

    Pathways

    Sensory Perception of Sound, Positive Regulation of Response to DNA Damage Stimulus
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