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CDH23 anticorps
CDH23
Reactivité: Humain, Souris, Rat
ELISA, WB, IHC
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN7235435
Détail du produit anti-CDH23 anticorps
(cache)
Antigène
Voir toutes CDH23 Anticorps
CDH23
(Cadherin 23 (CDH23))
Reactivité
Toutes les réactivités sur CDH23 Anticorps
Humain, Souris, Rat
Hôte
Toutes les hôtes sur CDH23 Anticorps
Lapin
Clonalité
Toutes les clonalités sur CDH23 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers CDH23 Anticorps
Cet anticorp CDH23 est non-conjugé
Application
Tous les applications à travers CDH23 Anticorps.
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
Attributs du produit
Polyclonal Antibody
Purification
Affinity purification
Immunogène
Recombinant protein of human CDH23
Isotype
IgG
Alternatives
(show)
Information d'application
(cache)
Indications d'application
WB 1:500-1:2000, IHC 1:100-1:300
Restrictions
For Research Use only
Stockage
(cache)
Format
Liquid
Concentration
0.4 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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 CDH23
(cache)
Antigène
CDH23
(Cadherin 23 (CDH23))
Autre désignation
Otocadherin (CDH23 Produits )
Synonymes
anticorps 4930542A03Rik, anticorps USH1D, anticorps ahl, anticorps ahl1, anticorps bob, anticorps bus, anticorps mdfw, anticorps nmf112, anticorps nmf181, anticorps nmf252, anticorps sals, anticorps v, anticorps CDHR23, anticorps W, anticorps cadherin 23 (otocadherin), anticorps cadherin related 23, anticorps cadherin-related 23, anticorps Cdh23, anticorps CDH23
Sujet
This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Alternative splice variants encoding different isoforms have been described.
Poids moléculaire
45 kDa
UniProt
Q9H251
Pathways
Sensory Perception of Sound
Vus récemment
(cache)