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TMEM67 antibody (C-Term)

TMEM67 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5517188
  • Target See all TMEM67 Antibodies
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Binding Specificity
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    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)
    Sequence
    FDLLFFCVVD LACQNFILAS FLTYLQQEIF RYIRNTVGQK NLASKTLVDQ
    Purification
    Affinity purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the C terminal region of human TMEM67
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    Discover our top product TMEM67 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Alternative Name
    TMEM67 (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).

    Alias Symbols: MKS3, JBTS6, NPHP11, TNEM67, MECKELIN,

    Protein Size: 995
    Gene ID
    91147
    NCBI Accession
    NM_001142301, NP_001135773
    UniProt
    Q5HYA8
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