K1C9 Polyclonal Antibody, 50ul Insect Expression Bardet-Biedl syndrome is an autosomal

Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy

The encoded protein is also involved in the control of microtubule stability during cytokinesis

and for cells involved in the expansion of T cells and dendritic cells which play an important role in immune surveillance

and has a preferred 5-kinase activity

K1C9 Polyclonal Antibody, 50ul Insect Expression Bardet-Biedl syndrome is an autosomalThis gene encodes the type I keratin 9, an intermediate filament chain expressed only in the terminally differentiated epidermis of palms and soles. Mutations in this gene cause epidermolytic palmoplantar keratoderma.