WB, ICC/IF, IHC, IHC-Fr, IHC-PHost:
Host: Rabbit Polyclonal
Meckelin localizes to the primary cilium and to the plasma membrane. It functions in centriole migration to the apical membrane and formation of the primary cilium. Defects in the gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).
|Product By Gene ID
- meckel syndrome type 3 protein
- transmembrane protein 67
Bioinformatics Tool for Meckelin
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