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Magic™ Membrane Protein Human TMEM67 (Transmembrane protein 67) Full Length (CAT#: MPC1620K) Made to Order

Datasheet
This product is a 111.7 kDa Human TMEM67 membrane protein expressed in HEK293. The protein is for research use only and is not approved for use in humans or in clinical diagnosis.

Product Specifications

  • Host Species
  • Human
  • Target Protein
  • TMEM67
  • Protein Length
  • Full length
  • Protein Class
  • Transporter
  • Molecular Weight
  • 111.7 kDa
  • TMD
  • 6
  • Sequence
  • MATRGGAGVAMAVWSLLSARAVTAFLLLFLPRFLQAQTFSFPFQQPEKCD
    NNQYFDISALSCVPCGANQRQDARGTSCVCLPGFQMISNNGGPAIICKKC
    PENMKGVTEDGWNCISCPSDLTAEGKCHCPIGHILVERDINGTLLSQATC
    ELCDGNENSFMVVNALGDRCVRCEPTFVNTSRSCACSEPNILTGGLCFSS
    TGNFPLRRISAARYGEVGMSLTSEWFAKYLQSSAAACWVYANLTSCQALG
    NMCVMNMNSYDFATFDACGLFQFIFENTAGLSTVHSISFWRQNLPWLFYG
    DQLGLAPQVLSSTSLPTNFSFKGENQNTKLKFVAASYDIRGNFLKWQTLE
    GGVLQLCPDTETRLNAAYSFGTTYQQNCEIPISKILIDFPTPIFYDVYLE
    YTDENQHQYILAVPVLNLNLQHNKIFVNQDSNSGKWLLTRRIFLVDAVSG
    RENDLGTQPRVIRVATQISLSVHLVPNTINGNIYPPLITIAYSDIDIKDA
    NSQSVKVSFSVTYEMDHGEAHVQTDIALGVLGGLAVLASLLKTAGWKRRI
    GSPMIDLQTVVKFLVYYAGDLANVFFIITVGTGLYWLIFFKAQKSVSVLL
    PMPIQEERFVTYVGCAFALKALQFLHKLISQITIDVFFIDWERPKGKVLK
    AVEGEGGVRSATVPVSIWRTYFVANEWNEIQTVRKINSLFQVLTVLFFLE
    VVGFKNLALMDSSSSLSRNPPSYIAPYSCILRYAVSAALWLAIGIIQVVF
    FAVFYERFIEDKIRQFVDLCSMSNISVFLLSHKCFGYYIHGRSVHGHADT
    NMEEMNMNLKREAENLCSQRGLVPNTDGQTFEIAISNQMRQHYDRIHETL
    IRKNGPARLLSSSASTFEQSIKAYHMMNKFLGSFIDHVHKEMDYFIKDKL
    LLERILGMEFMEPMEKSIFYNDEGYSFSSVLYYGNEATLLIFDLLFFCVV
    DLACQNFILASFLTYLQQEIFRYIRNTVGQKNLASKTLVDQRFLI

Product Description

  • Expression Systems
  • HEK293
  • Tag
  • Flag-StrepII or based on specific requirements
  • Protein Format
  • Detergent or based on specific requirements

Target

  • Target Protein
  • TMEM67
  • Full Name
  • Transmembrane protein 67
  • Introduction
  • 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).
  • Alternative Names
  • TMEM67; MKS3; JBTS6; NPHP11; TNEM67; MECKELIN; meckelin; meckel syndrome type 3 protein; Transmembrane protein 67

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