Anti-MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody is validated on Xenopus tissue and recommended for immunofluorescence labeling, IHC, or western blot of materials from Xenopus tissues.
Meckel syndrome, type 3 (MKS3) or TMEM67 or Meckelin or NPHP11 is encoded by the TMEM67 gene in Xenopus. MKS3 is a membrane protein containing 6 transmembrane domains. MKS3 is localized to the primary cilium functions in centriole migration to the apical membrane and formation of the primary cilium.
Mutations in TMEM67 cause Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6) (OMIM 607361).
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