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Tricellulin anticorps

MARVELD2 Reactivité: Humain, Rat, Souris WB, IHC, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7120257
  • Antigène Voir toutes Tricellulin (MARVELD2) Anticorps
    Tricellulin (MARVELD2)
    Reactivité
    • 31
    • 11
    • 10
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 31
    Lapin
    Clonalité
    • 31
    Polyclonal
    Conjugué
    • 14
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Tricellulin est non-conjugé
    Application
    • 23
    • 14
    • 14
    • 3
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Purification
    Immunogen affinity purified
    Pureté
    ≥95 % as determined by SDS-PAGE
    Immunogène
    MARVEL domain containing 2
    Isotype
    IgG
    Top Product
    Discover our top product MARVELD2 Anticorps primaire
  • Indications d'application
    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
    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
    Tricellulin (MARVELD2)
    Autre désignation
    MARVELD2 (MARVELD2 Produits)
    Synonymes
    anticorps Mrvldc2, anticorps BC003296, anticorps MARVD2, anticorps Tric, anticorps Trica, anticorps Tricb, anticorps Tricc, anticorps DFNB49, anticorps MRVLDC2, anticorps MARVEL domain containing 2, anticorps MARVEL (membrane-associating) domain containing 2, anticorps Marveld2, anticorps MARVELD2
    Sujet
    Synonyms:TRIC Background:The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene.
    Poids moléculaire
    69 kDa
    ID gène
    153562
    UniProt
    Q8N4S9
    Pathways
    Sensory Perception of Sound, Cell-Cell Junction Organization
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