Recombinant fusion protein of human TMEM67(NP_714915.3).
Conjugation:
Unconjugated
Alternative Names:
TMEM67,JBTS6,MECKELIN,MKS3,NPHP11,TNEM67,meckelin
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).
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Form:
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Application Dilute:
WB,1:200 - 1:2000
Application Notes:
Unmodification
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