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ZIC3 anticorps (AA 113-455)

Cet anticorps anti-ZIC3 Polyclonal Lapin (ABIN7870153) détecte spécifiquement ZIC3 dans WB, ELISA et FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7870153
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour ZIC3 anticorps (AA 113-455) (ABIN7870153)

Antigène

Voir toutes ZIC3 Anticorps
ZIC3 (Zic Family Member 3 (ZIC3))

Reactivité

  • 30
  • 12
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 23
  • 5
  • 2
Lapin

Clonalité

  • 25
  • 5
Polyclonal

Conjugué

  • 23
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ZIC3 est non-conjugé

Application

  • 19
  • 9
  • 8
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Épitope

    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 113-455

    Fonction

    ZIC3 Antibody

    Purification

    Antigen affinity purified

    Immunogène

    Recombinant human protein (amino acids N113-N455) was used as the immunogen for the ZIC3 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the ZIC3 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 ZIC3 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

    ZIC3 (Zic Family Member 3 (ZIC3))

    Autre désignation

    ZIC3

    Sujet

    ZIC3 is a member of the Zinc finger of the cerebellum (ZIC) protein family. This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. This nuclear protein probably functions as a transcription factor in early stages of left-right body axis formation. Mutations in this gene cause X-linked visceral heterotaxy, which includes congenital heart disease and left-right axis defects in organs.

    UniProt

    O60481
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