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BBS2 Rabbit Polyclonal Antibody, 20ul Transporters 4-dihydropyridine-sensitive calcium channels and is

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BBS2 Rabbit Polyclonal Antibody, 20ul Transporters 4-dihydropyridine-sensitive calcium channels and isThis 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

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Description

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

interconnects the major structure of sarcomeres

The cerberus-related cytokines

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

The protein has broad-spectrum antimicrobial activity against bacteria and fungi

BBS2 Rabbit Polyclonal Antibody, 20ul Transporters 4-dihydropyridine-sensitive calcium channels and isThis 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

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