BBS10 is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded ...
Cat # 15751382
100 µL
Cat # 16830134
20 µL
Cat # 16820134
150 µL
Cat # 16838785
150 µL
Cat # 13290039
100 µL
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100 µL
Cat # 16636614
100 µL
Cat # 16848785
20 µL
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