BBS2 Rabbit Polyclonal Antibody, 20ul Transporters releasing free sphingoid base that

releasing free sphingoid base that functions as an endogenous antimicrobial agent

Its predicted protein sequence differs significantly from the known functional trypsinogens| including a different amino acid at the conserved residue 122 which is important for autolysis

4-dihydropyridine-sensitive calcium channels and is an integral membrane protein that plays a role in excitation-contraction coupling

An important paralog of this gene is RPL7

LIMK1 is a serine/threonine kinase that regulates actin polymerization via phosphorylation and inactivation of the actin binding factor cofilin

BBS2 Rabbit Polyclonal Antibody, 20ul Transporters releasing free sphingoid base thatThis 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