Anti-BBS7 antibody is validated on mouse tissue and recommended for immunofluorescence labeling, IHC, or western blot of materials from rodent and human tissues.
Bardet-Biedl syndrome 7 (BBS7) protein, is encoded by the BBS7 gene in human. The BBS7 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 BBS7 are linked to Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy (OMIM 615984).
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