PKD1/2/3(Phospho Ser738/S742) Polyclonal Antibody, 20ul Virus Packaging Mutations in TP63 are associated

Mutations in TP63 are associated with ectodermal dysplasia

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

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

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

Arginine methylation is an apparently irreversible protein modification catalyzed by arginine methyltransferases

PKD1/2/3(Phospho Ser738/S742) Polyclonal Antibody, 20ul Virus Packaging Mutations in TP63 are associatedPRKD1 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