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FOXI1 anticorps (AA 224-253)

L’anticorps Lapin Polyclonal anti-FOXI1 a été validé pour WB. Il convient pour détecter FOXI1 dans des échantillons de Humain.
N° du produit ABIN656114

Aperçu rapide pour FOXI1 anticorps (AA 224-253) (ABIN656114)

Antigène

Voir toutes FOXI1 Anticorps
FOXI1 (Forkhead Box I1 (FOXI1))

Reactivité

  • 47
  • 9
  • 6
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Humain

Hôte

  • 41
  • 5
  • 1
Lapin

Clonalité

  • 44
  • 3
Polyclonal

Conjugué

  • 24
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FOXI1 est non-conjugé

Application

  • 27
  • 18
  • 13
  • 13
  • 8
  • 7
  • 4
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB)

Clone

RB32223
  • Épitope

    • 15
    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 224-253

    Purification

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

    Immunogène

    This FOXI1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 224-253 amino acids from the Central region of human FOXI1.

    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

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Date de péremption

    6 months
  • Antigène

    FOXI1 (Forkhead Box I1 (FOXI1))

    Autre désignation

    FOXI1

    Sujet

    This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined, however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    40973

    ID gène

    2299

    NCBI Accession

    NP_036320, NP_658982

    UniProt

    Q12951
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