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OFD1 anticorps

Cet anticorps anti-OFD1 Polyclonal Lapin (ABIN7881878) détecte spécifiquement OFD1 dans WB, IF et FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7881878
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour OFD1 anticorps (ABIN7881878)

Antigène

Voir toutes OFD1 Anticorps
OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))

Reactivité

  • 17
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 17
Lapin

Clonalité

  • 17
Polyclonal

Conjugué

  • 13
  • 2
  • 1
  • 1
Cet anticorp OFD1 est non-conjugé

Application

  • 12
  • 7
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)
  • Fonction

    OFD1 Antibody / Oral-facial-digital syndrome 1

    Séquence

    KDKSAHSENP LEKYMKIIQQ EQDQESADK

    Purification

    Affinity purified

    Immunogène

    Amino acids KDKSAHSENPLEKYMKIIQQEQDQESADK from the human protein were used as the immunogen for the OFD1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the OFD1 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 OFD1 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

    OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))

    Autre désignation

    OFD1

    Sujet

    Oral-facial-digital syndrome 1 protein is a protein that in humans is encoded by the OFD1 gene. This gene is mapped to Xp22.2. This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified, a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome.

    UniProt

    O75665

    Pathways

    M Phase
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