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TMCO1 Protein (Myc-DYKDDDDK Tag)

TMCO1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2733829
  • Target See all TMCO1 Proteins
    TMCO1 (Transmembrane and Coiled-Coil Domains 1 (TMCO1))
    Protein Type
    Recombinant
    Origin
    • 2
    • 1
    Human
    Source
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This TMCO1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human TMCO1 / TMCC4 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 TMCO1 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
    TMCO1 (Transmembrane and Coiled-Coil Domains 1 (TMCO1))
    Alternative Name
    Tmco1,tmcc4 (TMCO1 Products)
    Synonyms
    DKFZp459A2226 Protein, sb:cb729 Protein, zgc:110322 Protein, zgc:92740 Protein, HP10122 Protein, PCIA3 Protein, PNAS-136 Protein, RP11-466F5.7 Protein, TMCC4 Protein, 1190006A08Rik Protein, 4930403O06Rik Protein, AA109065 Protein, AU022572 Protein, ESTM39 Protein, transmembrane and coiled-coil domains 1 Protein, transmembrane and coiled-coil domains 1 S homeolog Protein, TMCO1 Protein, tmco1 Protein, tmco1.S Protein, Tmco1 Protein
    Background
    This locus encodes a transmembrane protein. Mutations at this locus have been associated with craniofacial dysmorphism, skeletal anomalies, and mental retardation. Mutations at this locus have also been associated with open angle glaucoma blindness. Alternatively spliced transcript variants have been described.
    Molecular Weight
    21 kDa
    NCBI Accession
    NP_061899
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