BBS2 Rabbit Polyclonal Antibody, 50ul 3D Culture Ehlers-Danlos syndrome type VIIB

Ehlers-Danlos syndrome type VIIB

and is involved in B-cell proliferation and immunoglobulin secretion

enzyme regulation:Inhibited by cGMP

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

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

BBS2 Rabbit Polyclonal Antibody, 50ul 3D Culture Ehlers-Danlos syndrome type VIIBThis 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