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FOXL2 anticorps

L’anticorps anti-FOXL2 Polyclonal Lapin est utilisé pour la détection de FOXL2 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, FACS et IHC (p).
N° du produit ABIN7880811
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour FOXL2 anticorps (ABIN7880811)

Antigène

Voir toutes FOXL2 Anticorps
FOXL2 (Forkhead Box L2 (FOXL2))

Reactivité

  • 86
  • 38
  • 25
  • 20
  • 19
  • 17
  • 6
  • 5
  • 2
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 79
  • 8
  • 1
Lapin

Clonalité

  • 64
  • 24
Polyclonal

Conjugué

  • 56
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FOXL2 est non-conjugé

Application

  • 54
  • 30
  • 16
  • 12
  • 11
  • 11
  • 6
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Fonction

    FOXL2 Antibody

    Séquence

    ACARQPELAM MHCSYWDHD

    Purification

    Antigen affinity purified

    Immunogène

    Amino acids ACARQPELAMMHCSYWDHD from the human protein were used as the immunogen for the FOXL2 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the FOXL2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the FOXL2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    FOXL2 (Forkhead Box L2 (FOXL2))

    Autre désignation

    FOXL2

    Sujet

    The forkhead transcription factor gene, FOXL2 located in blepharophimosis, ptosis and epicanthus inversus syndrome (BPES) critical region on chromosome 3q23. Consistent with an involvement in BPES, FOXL2 is selectively expressed in the mesenchyme of developing mouse eyelids and in adult ovarian follicles, in adult humans, it appears predominantly in the ovary. FOXL2 haploinsufficiency may cause BPES types I and II by the effect of a null allele and a hypomorphic allele, respectively. Furthermore, in a fraction of the BPES patients the genetic defect does not reside within the coding region of the FOXL2 gene and may be caused by a position effect. FOXL2 mutations can also cause gonadal dysgenesis or premature ovarian failure(POF) in women, as well as eyelid/forehead dysmorphology in both sexes.

    UniProt

    P58012

    Pathways

    Nuclear Hormone Receptor Binding, Positive Regulation of Endopeptidase Activity
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