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Protein structure
TMEM67
Transmembrane protein 67JBTS6, MGC26979, MKS3, NPHP11
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, Nov 2008]
Top validated antibodies |
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| Proteintech Group |  13975-1-AP |
22 references | Polyclonal |
EL
ICC
IHC
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| Novus Biologicals | NBP1-06590 |
1 references | Polyclonal |
WB
ICC
IHC
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| Biorbyt | orb1147240 |
Monoclonal |
WB
ICC
IHC
FC
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| Invitrogen Antibodies | PA5-141155 |
Polyclonal |
WB
IHC
FC
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| OriGene | AP55072SU-N |
Polyclonal |
WB
EL
IHC
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