Anti-BBS8 (TTC8) antibody is validated on mouse tissue and can be used for immunofluorescence labeling, IHC, or western blot of materials from rodent and human tissues.
Bardet-Biedl syndrome 8 (BBS8) protein, also known as Tetratricopeptide report domain 8 (TTC8), is encoded by the TTC8 gene in human. The BBS8 protein participates in the formation of the BBSome complex. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis.
Mutations in BBS8 are linked to Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy (OMIM 615985).
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