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Tricellulin anticorps

MARVELD2 Reactivité: Humain, Rat, Souris WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6571916
  • Antigène Voir toutes Tricellulin (MARVELD2) Anticorps
    Tricellulin (MARVELD2)
    Reactivité
    • 32
    • 12
    • 11
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 32
    Lapin
    Clonalité
    • 32
    Polyclonal
    Conjugué
    • 15
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Tricellulin est non-conjugé
    Application
    • 24
    • 15
    • 15
    • 3
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogène
    A synthetic peptide of human MARVELD2 (NP_001033692.2).
    Isotype
    IgG
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    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
    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.
  • 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
    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

    Observed_MW: Refer to figures

    Calculated_MW: 51kDa/62kDa/64kDa

    ID gène
    153562
    UniProt
    Q8N4S9
    Pathways
    Sensory Perception of Sound, Cell-Cell Junction Organization
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