BBS2 Rabbit Polyclonal Antibody, 50ul 3D Culture and the adenovirus E1A-associated cellular

and the adenovirus E1A-associated cellular p300 transcriptional co-activator protein

Ehlers-Danlos syndrome type VIIB

Mitotic and Regulation of PLK1 Activity at G2/M Transition

ensuring accurate and safe pipetting

Omega-3 fatty acid receptor 1 functions as a receptor for free fatty acids

BBS2 Rabbit Polyclonal Antibody, 50ul 3D Culture and the adenovirus E1A-associated cellularThis gene is a member of the Bardet Biedl syndrome (BBS) gene family. Bardet Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and