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Tricellulin Protein (MARVELD2) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

MARVELD2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2734221
  • Antigène Voir toutes Tricellulin (MARVELD2) Protéines
    Tricellulin (MARVELD2)
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 1
    Origine
    • 3
    • 3
    Humain
    Source
    • 2
    • 2
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette Tricellulin protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Tricellulin (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MARVELD2 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    Tricellulin (MARVELD2)
    Autre désignation
    Tricellulin (MARVELD2 Produits)
    Synonymes
    Mrvldc2 Protein, BC003296 Protein, MARVD2 Protein, Tric Protein, Trica Protein, Tricb Protein, Tricc Protein, DFNB49 Protein, MRVLDC2 Protein, MARVEL domain containing 2 Protein, MARVEL (membrane-associating) domain containing 2 Protein, Marveld2 Protein, MARVELD2 Protein
    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
    64 kDa
    NCBI Accession
    NP_001033692
    Pathways
    Sensory Perception of Sound, Cell-Cell Junction Organization
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