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EYA1 anticorps (N-Term)

Cet anticorps anti-EYA1 est un anticorps Lapin Polyclonal détectant EYA1 dans WB. Adapté pour Souris.
N° du produit ABIN656379

Aperçu rapide pour EYA1 anticorps (N-Term) (ABIN656379)

Antigène

Voir toutes EYA1 Anticorps
EYA1 (Eyes Absent Homolog 1 (EYA1))

Reactivité

  • 35
  • 18
  • 8
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
Souris

Hôte

  • 39
  • 1
  • 1
Lapin

Clonalité

  • 41
Polyclonal

Conjugué

  • 18
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp EYA1 est non-conjugé

Application

  • 21
  • 18
  • 13
  • 13
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB31192
  • Épitope

    • 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.

    Immunogène

    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
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.

    Date de péremption

    6 months
  • Antigène

    EYA1 (Eyes Absent Homolog 1 (EYA1))

    Autre désignation

    EYA1

    Sujet

    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.

    Poids moléculaire

    64593

    ID gène

    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
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