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Rho-related GTP-binding protein anticorps
RhO (pan)
Reactivité: Souris, Rat
IHC
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN7258362
Détail du produit anti-Rho-related GTP-binding protein anticorps
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Antigène
Voir toutes Rho-related GTP-binding protein (RhO (pan)) Anticorps
Rho-related GTP-binding protein (RhO (pan))
Reactivité
Toutes les réactivités sur Rho-related GTP-binding protein Anticorps
Souris, Rat
Hôte
Toutes les hôtes sur Rho-related GTP-binding protein Anticorps
Lapin
Clonalité
Toutes les clonalités sur Rho-related GTP-binding protein Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers Rho-related GTP-binding protein Anticorps
Cet anticorp Rho-related GTP-binding protein est non-conjugé
Application
Tous les applications à travers Rho-related GTP-binding protein Anticorps.
Immunohistochemistry (IHC)
Attributs du produit
Polyclonal Antibody
Purification
Affinity purification
Immunogène
A synthetic peptide of human RHO (NP_000530.1).
Isotype
IgG
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Information d'application
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Indications d'application
IHC 1:50-1:200
Restrictions
For Research Use only
Stockage
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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.
Détails sur Rho-related GTP-binding protein
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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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