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TMEM67 antibody

TMEM67 Reactivity: Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1112910
  • Target See all TMEM67 Antibodies
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Reactivity
    • 19
    • 3
    • 1
    Mouse
    Host
    • 20
    Rabbit
    Clonality
    • 20
    Polyclonal
    Conjugate
    • 10
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TMEM67 antibody is un-conjugated
    Application
    • 8
    • 6
    • 4
    • 2
    Western Blotting (WB)
    Purification
    affinity purified
    Isotype
    IgG
    Top Product
    Discover our top product TMEM67 Primary Antibody
  • Application Notes
    WB (1:500). Other applications have not been tested. The optimal dilutions should be determined by end user.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    TBS (pH7.4), 0.5% BSA, 40% Glycerol and 0.05% Sodium Azide.
    Preservative
    Sodium azide, Thimerosal (Merthiolate)
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at 4 °C after thawing (1 week). Aliquot and store at -20 °C for long term (at least one year). Avoid repeated freeze and thaw cycles.
    Expiry Date
    12 months
  • Target
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Alternative Name
    Meckelin (TMEM67 Products)
    Synonyms
    JBTS6 antibody, MECKELIN antibody, MKS3 antibody, NPHP11 antibody, TNEM67 antibody, 5330408M12Rik antibody, B230117O07 antibody, b2b1163.1Clo antibody, b2b1291.1Clo antibody, Wpk antibody, transmembrane protein 67 antibody, TMEM67 antibody, tmem67 antibody, Tmem67 antibody
    Background
    Meckelin, also called Transmembrane protein 67 (TMEM67), which encoded by the TMEM67 gene, is a 995-amino acid protein, localizes to the primary cilium and to the plasma membrane. Using in situ hybridization with human embryos, Dawe et al. (2007) found that meckelin was expressed in kidney, liver, retina, hindbrain, developing sphenoid bone, and the brain midline. The lack of this protein will cause Meckel syndrome type 3 (MKS3) , nephronophthisis and Joubert syndrome type 6 (JBTS6).
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