PKD1(Phospho Tyr463) Polyclonal Antibody, 50ul Cell Function Analysis Defects in this gene are

Defects in this gene are cause of an autosomal recessive cutis laxa syndrome

also known as 5-azacytidine-induced protein 1

May play a direct role in a TNF-alpha signaling pathway leading to induction of cell death

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 Defects in this gene arePRKD1 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