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

MARVELD2 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2734221
  • Target See all Tricellulin (MARVELD2) Proteins
    Tricellulin (MARVELD2)
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 1
    Origin
    • 3
    • 3
    Human
    Source
    • 3
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This Tricellulin protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Tricellulin (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MARVELD2 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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)
    Alternative Name
    Tricellulin (MARVELD2 Products)
    Synonyms
    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
    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.
    Molecular Weight
    64 kDa
    NCBI Accession
    NP_001033692
    Pathways
    Sensory Perception of Sound, Cell-Cell Junction Organization
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