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Rho-related GTP-binding protein anticorps

L’anticorps Lapin Polyclonal anti-Rho-related GTP-binding protein a été validé pour IHC. Il convient pour détecter Rho-related GTP-binding protein dans des échantillons de Rat et Souris.
N° du produit ABIN7258362

Aperçu rapide pour Rho-related GTP-binding protein anticorps (ABIN7258362)

Antigène

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

Reactivité

  • 16
  • 7
  • 7
  • 6
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Rat, Souris

Hôte

  • 20
  • 8
  • 1
Lapin

Clonalité

  • 18
  • 11
Polyclonal

Conjugué

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

Application

  • 22
  • 19
  • 15
  • 6
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    A synthetic peptide of human RHO (NP_000530.1).

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 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.

    ID gène

    6010

    UniProt

    P08100
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