BBS2 Rabbit Polyclonal Antibody, 50ul 3D Culture subunit:Heterotetramer

subunit:Heterotetramer

and is involved in B-cell proliferation and immunoglobulin secretion

Ehlers-Danlos syndrome type VIIB

Fibroblast growth factor 11 encoded by FGF11 is a member of the fibroblast growth factor (FGF) family

Mitotic and Regulation of PLK1 Activity at G2/M Transition

BBS2 Rabbit Polyclonal Antibody, 50ul 3D Culture subunit:HeterotetramerThis 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