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PCDH15 anticorps

PCDH15 Reactivité: Humain, Souris, Rat WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7118101
  • Antigène Voir toutes PCDH15 Anticorps
    PCDH15 (Protocadherin-15 (PCDH15))
    Reactivité
    • 13
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 10
    • 3
    • 2
    Lapin
    Clonalité
    • 13
    • 2
    Polyclonal
    Conjugué
    • 15
    Cet anticorp PCDH15 est non-conjugé
    Application
    • 12
    • 7
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA
    Purification
    Immunogen affinity purified
    Pureté
    ≥95 % as determined by SDS-PAGE
    Immunogène
    PCDH15
    Isotype
    IgG
    Top Product
    Discover our top product PCDH15 Anticorps primaire
  • Indications d'application
    WB: 1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide and 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
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    Date de péremption
    12 months
  • Antigène
    PCDH15 (Protocadherin-15 (PCDH15))
    Autre désignation
    PCDH15 (PCDH15 Produits)
    Synonymes
    anticorps CDHR15, anticorps DFNB23, anticorps USH1F, anticorps BB078305, anticorps ENSMUSG00000046980, anticorps Gm9815, anticorps Ush1f, anticorps av, anticorps nmf19, anticorps protocadherin-15, anticorps protocadherin related 15, anticorps protocadherin-15, anticorps protocadherin 15, anticorps PCDH15, anticorps CpipJ_CPIJ005081, anticorps Pcdh15
    Sujet
    Synonyms:CDHR15, DFNB23, USH1F, PCD15 Background:This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur.
    Poids moléculaire
    100kDa
    ID gène
    65217
    UniProt
    Q96QU1
    Pathways
    Sensory Perception of Sound
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