Anti-BBS4 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 4 (BBS4) protein is encoded by the BBS4 gene in human. The BBS4 protein contains multiple tetratricopeptide repeats (TPR). The BBS4 protein plays a vital role in the formation of the centrosome.
Mutations in BBS4 cause Bardet–Biedl syndrome, an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation, and mental retardation (OMIM 615982).
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