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

MARVELD2 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2734221
  • Target Alle Tricellulin (MARVELD2) Proteine anzeigen
    Tricellulin (MARVELD2)
    Protein-Typ
    Recombinant
    Proteineigenschaft
    Transcript Variant 1
    Spezies
    • 3
    • 3
    Human
    Quelle
    • 2
    • 2
    • 2
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses Tricellulin Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Tricellulin (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MARVELD2 Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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.
  • Target
    Tricellulin (MARVELD2)
    Andere Bezeichnung
    Tricellulin (MARVELD2 Produkte)
    Synonyme
    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
    Hintergrund
    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.
    Molekulargewicht
    64 kDa
    NCBI Accession
    NP_001033692
    Pathways
    Sensory Perception of Sound, Cell-Cell Junction Organization
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