PKD1(Phospho Tyr463) Polyclonal Antibody, 50ul Cell Function Analysis Mutations in TUBB3 are the

Mutations in TUBB3 are the cause of congenital fibrosis of the extraocular muscles type 3

also known as 5-azacytidine-induced protein 1

As a scaffold protein involved in cell polarization processes| this protein binds to many other proteins

coli AlkB homologs that catalyze the removal of 1-methyladenine and 3-methylcytosine (Duncan et al

PKD1(Phospho Tyr463) Polyclonal Antibody, 50ul Cell Function Analysis Mutations in TUBB3 are thePRKD1 is a serine threonine kinase that regulates a variety of cellular functions, including membrane receptor signaling, transport at the Golgi, protection from oxidative stress at the mitochondria, gene transcription, and regulation of cell shape, motility, and adhesion (summary by Eiseler et al., 2009