PKA I Alpha reg Polyclonal Antibody, 100ul Immune Cell Analysis Bardet-Biedl syndrome is an autosomal

Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy

The protein encoded by this gene belongs to the Rab family

and the longer isoform contains nine C2H2-type zinc finger repeats in the C-terminal domain

all variants encode the same N-terminus

Gene synthesis is widely applied in various fields

PKA I Alpha reg Polyclonal Antibody, 100ul Immune Cell Analysis Bardet-Biedl syndrome is an autosomalcAMP is a signaling molecule important for a variety of cellular functions. cAMP exerts its effects by activating the cAMP dependent protein kinase, which transduces the signal through phosphorylation of different target proteins. The inactive kinase holoenzyme is a tetramer composed of two regulatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free