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Pejvakin anticorps (AA 170-197)
DFNB59
Reactivité: Humain
WB
Hôte: Lapin
Polyclonal
RB37747
unconjugated
N° du produit ABIN1537942
Détail du produit anti-Pejvakin anticorps
(cache)
Antigène
Voir toutes Pejvakin (DFNB59) Anticorps
Pejvakin (DFNB59)
(Deafness, Autosomal Recessive 59 (DFNB59))
Épitope
Tous les épitopes à travers Pejvakin Anticorps.
AA 170-197
Reactivité
Humain
Hôte
Toutes les hôtes sur Pejvakin Anticorps
Lapin
Clonalité
Toutes les clonalités sur Pejvakin Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers Pejvakin Anticorps
Cet anticorp Pejvakin est non-conjugé
Application
Tous les applications à travers Pejvakin Anticorps.
Western Blotting (WB)
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Immunogène
This PJVK antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 170-197 amino acids from the Central region of human PJVK.
Clone
RB37747
Isotype
Ig Fraction
Alternatives
(show)
Information d'application
(cache)
Indications d'application
WB: 1:1000
Restrictions
For Research Use only
Stockage
(cache)
Format
Liquid
Buffer
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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
4 °C,-20 °C
Stockage commentaire
PJVK Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
Date de péremption
6 months
Détails sur Pejvakin
(cache)
Antigène
Pejvakin (DFNB59)
(Deafness, Autosomal Recessive 59 (DFNB59))
Autre désignation
PJVK (DFNB59 Produits )
Synonymes
anticorps PJVK, anticorps Gm1001, anticorps Pjvk, anticorps deafness, autosomal recessive 59, anticorps pejvakin, anticorps DFNB59, anticorps PJVK, anticorps Pjvk
Sujet
The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59).
Poids moléculaire
39913
ID gène
494513
NCBI Accession
NP_001036167
UniProt
Q0ZLH3
Pathways
Sensory Perception of Sound
Vus récemment
(cache)