PKD1/2/3(Phospho Ser738/S742) Polyclonal Antibody, 20ul Virus Packaging Mutations in this gene cause

Mutations in this gene cause the disorder trimethylaminuria (TMAu) which is characterized by the accumulation and excretion of unmetabolized trimethylamine and a distinctive body odor

It encodes a single-pass type I membrane protein with multiple cysteine rich domains

and thus inhibits the synthesis of proinflammatory cytokines

DQX1 is encoded by a gene that maps to human chomosome 2

This peptide is a potent vasoconstrictor and its cognate receptors are therapeutic targets in the treatment of pulmonary arterial hypertension

PKD1/2/3(Phospho Ser738/S742) Polyclonal Antibody, 20ul Virus Packaging Mutations in this gene causePRKD1 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