EST1 Rabbit Polyclonal Antibody, 20ul Purification Mutations in PLN are a

Mutations in PLN are a cause of inherited human dilated cardiomyopathy with refractory congestive heart failure

GO annotations related to this gene include receptor activity and scavenger receptor activity

promotes the hydrolysis of bound GTP and hence returns RAP1 to the inactive state whereas other proteins

This transcription factor functions as a negative regulator of epithelial cell growth in prostate tissue

adhesion to fibrinogen matrix proteins

EST1 Rabbit Polyclonal Antibody, 20ul Purification Mutations in PLN are aThis 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 may participate in fatty acyl and cholesterol ester metabolism and may play a role in the blood brain barrier system. This enzyme is the major liver enzyme and functions in liver drug clearance.