EST5A Rabbit Polyclonal Antibody, 100ul Dialysis a common congenital disorder characterized

a common congenital disorder characterized by neural-crest-related developmental defects

and acts as a decoy receptor that inhibits the activity of its ligands

Interacts with PPP1C and HNRPK

Three related pseudogenes are located within the Smith-Magenis syndrome region on chromosome 17

EST5A Rabbit Polyclonal Antibody, 100ul Dialysis a common congenital disorder characterizedThis gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics such as cocaine and heroin and endogenous substrates with ester thioester or amide bonds. They also participate in fatty acyl and cholesterol ester metabolism and may play a role in the blood brain barrier system. This gene also called CES5 is predominantly expressed in peripheral tissues