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Rho-related GTP-binding protein anticorps

RhO (pan) Reactivité: Souris, Rat IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7258362
  • Antigène Voir toutes Rho-related GTP-binding protein (RhO (pan)) Anticorps
    Rho-related GTP-binding protein (RhO (pan))
    Reactivité
    • 18
    • 7
    • 7
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Souris, Rat
    Hôte
    • 22
    • 4
    • 1
    Lapin
    Clonalité
    • 22
    • 5
    Polyclonal
    Conjugué
    • 18
    • 3
    • 2
    • 2
    • 1
    • 1
    Cet anticorp Rho-related GTP-binding protein est non-conjugé
    Application
    • 21
    • 18
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    A synthetic peptide of human RHO (NP_000530.1).
    Isotype
    IgG
    Top Product
    Discover our top product RhO (pan) Anticorps primaire
  • 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 (RhO (pan) Produits)
    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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