Anti-BBS2 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 2 (BBS2) protein is encoded by the BBS2 gene in human. The function of BBS2 protein is unknown but suspected to play a role in the regulation of centrosomal formation.
Mutations in BBS2 cause Bardet–Biedl syndrome, an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation, and mental retardation (OMIM 615981).
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