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

EYA1 antibody (N-Term)

This anti-EYA1 antibody is a Rabbit Polyclonal antibody detecting EYA1 in WB. Suitable for Mouse.
Catalog No. ABIN656379

Quick Overview for EYA1 antibody (N-Term) (ABIN656379)

Target

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

Reactivity

  • 35
  • 18
  • 8
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
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
  • 1
Western Blotting (WB)

Clone

RB31192
  • Binding Specificity

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

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This EYA1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human EYA1.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

    Storage Comment

    EYA1 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Expiry Date

    6 months
  • 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.

    Molecular Weight

    64593

    Gene ID

    2138

    NCBI Accession

    NP_000494, NP_742055, NP_742056, NP_742057

    UniProt

    Q99502

    Pathways

    Sensory Perception of Sound, Positive Regulation of Response to DNA Damage Stimulus
You are here:
Chat with us!