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TMEM67 antibody (Isoform 1)

TMEM67 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1886737
  • Target See all TMEM67 Antibodies
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Binding Specificity
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Isoform 1
    Reactivity
    • 19
    • 3
    • 1
    Human
    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
    Purified by antigen-affinity chromatography.
    Immunogen
    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 231 and 480 of Human TMEM67
    Top Product
    Discover our top product TMEM67 Primary Antibody
  • Application Notes
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    Preservative
    Thimerosal (Merthiolate)
    Precaution of Use
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • 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
    The protein encoded by this gene localizes to the primary cilium and to the plasma membrane.The gene functions in centriole migration to the apical membrane and formation of the primary cilium.Multiple transcript variants encoding different isoforms have been found for this gene.Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).[provided by RefSeq]
    Molecular Weight
    112 kDa
    Gene ID
    91147
    NCBI Accession
    NP_714915, NM_153704
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