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

Rho-related GTP-binding protein anticorps

L’anticorps Lapin Monoclonal anti-Rho-related GTP-binding protein a été validé pour WB et IHC. Il convient pour détecter Rho-related GTP-binding protein dans des échantillons de Humain.
N° du produit ABIN7269974

Aperçu rapide pour Rho-related GTP-binding protein anticorps (ABIN7269974)

Antigène

Voir toutes Rho-related GTP-binding protein (RhO (pan)) Anticorps
Rho-related GTP-binding protein (RhO (pan))

Reactivité

  • 15
  • 8
  • 7
  • 7
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 20
  • 8
  • 1
Lapin

Clonalité

  • 19
  • 10
Monoclonal

Conjugué

  • 24
  • 2
  • 2
  • 1
Cet anticorp Rho-related GTP-binding protein est non-conjugé

Application

  • 21
  • 19
  • 15
  • 6
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Fonction

    Rhodopsin Rabbit mAb

     Réactivité croisée

    Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human Rhodopsin

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    Rho-related GTP-binding protein (RhO (pan))

    Autre désignation

    RHO

    Sujet

    Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness. [provided by RefSeq, Jul 2008],CSNBAD1, OPN2, RP4,G protein signaling,G protein signaling_G-Protein-Coupled Receptors(GPCR),Neuroscience,Signal Transduction,RHO

    Poids moléculaire

    39kDa

    ID gène

    6010

    UniProt

    P08100
Vous êtes ici:
Chat with us!