Anti-BBS9 (PTHB1) antibody is validated on mouse tissue and can be used for immunofluorescence labeling, IHC, or western blot of materials from rodent tissues.
Bardet-Biedl syndrome 9 (BBS9) protein, also known as parathyroid hormone responsive B1 gene (PTHB1), is encoded by the BBS9 gene in human. The BBS9 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.
The expression of BBS9 protein is downregulated by parathyroid hormone in osteoblastic cells. Mutations in BBS9 are linked to Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy (OMIM 615986).
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