Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

CRB1 anticorps

Cet anticorps anti-CRB1 Polyclonal Lapin (ABIN7880515) détecte spécifiquement CRB1 dans WB, IHC (p) et FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7880515
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour CRB1 anticorps (ABIN7880515)

Antigène

Voir toutes CRB1 Anticorps
CRB1 (Crumbs Homolog 1 (CRB1))

Reactivité

Humain, Souris, Rat

Hôte

  • 19
  • 1
Lapin

Clonalité

  • 20
Polyclonal

Conjugué

  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CRB1 est non-conjugé

Application

  • 13
  • 13
  • 6
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Fonction

    CRB1 Antibody

    Séquence

    FRTRDANVII LHAEKEPEFL NISIQDSRLF FQLQ

    Purification

    Affinity purified

    Immunogène

    Amino acids FRTRDANVIILHAEKEPEFLNISIQDSRLFFQLQ from the human protein were used as the immunogen for the CRB1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the CRB1 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

    -20 °C

    Stockage commentaire

    Store the CRB1 antibody at -20oC.
  • Antigène

    CRB1 (Crumbs Homolog 1 (CRB1))

    Autre désignation

    CRB1

    Sujet

    Crumbs homolog 1 is a protein that in humans is encoded by the CRB1 gene. This gene encodes a protein which is similar to the Drosophila crumbs protein and localizes to the inner segment of mammalian photoreceptors. In Drosophila crumbs localizes to the stalk of the fly photoreceptor and may be a component of the molecular scaffold that controls proper development of polarity in the eye. Mutations in this gene are associated with a severe form of retinitis pigmentosa, RP12, and with Leber congenital amaurosis. Alternate splicing results in multiple transcript variants, some protein coding and some non-protein coding.

    UniProt

    P82279

    Pathways

    Signalisation Notch
Vous êtes ici:
Chat with us!