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EYA1 anticorps (N-Term)

Cet anticorps anti-EYA1 est un anticorps Lapin Polyclonal détectant EYA1 dans WB et EIA. Adapté pour Humain et Souris.
N° du produit ABIN952149

Aperçu rapide pour EYA1 anticorps (N-Term) (ABIN952149)

Antigène

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

Reactivité

  • 34
  • 18
  • 8
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
Humain, 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
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Épitope

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

    Specificité

    This antibody recognizes Mouse EYA1 (N-term).

    Purification

    Affinity Chromatography on Protein A

    Immunogène

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

    Isotype

    Ig Fraction
  • Indications d'application

    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

    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.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 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.Synonyms: Eyes absent homolog 1

    Poids moléculaire

    64593 Da

    ID gène

    2138

    NCBI Accession

    NP_000494

    Pathways

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