TPH1(Phospho Ser58) Polyclonal Antibody, 20ul Dry Bath kidney and muscle

kidney and muscle

Dissociates from the centrioles at the onset of mitosis and reassociates with them at anaphase

The function of this protein has not been determined

Mutations in CREBBP cause Rubinstein-Taybi syndrome (RTS)

This gene is located within the Smith-Magenis syndrome region on chromosome 17

TPH1(Phospho Ser58) Polyclonal Antibody, 20ul Dry Bath kidney and muscleThis gene encodes a member of the aromatic amino acid hydroxylase family. The encoded protein catalyzes the first and rate limiting step in the biosynthesis of serotonin, an important hormone and neurotransmitter. Mutations in this gene have been associated with an elevated risk for a variety of diseases and disorders, including schizophrenia, somatic anxiety, anger related traits, bipolar disorder, suicidal behavior, addictions, and others.