HTRA1 Polyclonal Antibody, 50ul Molecular Biologyn Mutations in this gene cause

Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM)

uniform thickness

Enriched in synaptosomes

especially within the brain

A mutation in this gene results in one form of Zellweger syndrome

HTRA1 Polyclonal Antibody, 50ul Molecular Biologyn Mutations in this gene causeThis gene encodes a member of the trypsin family of serine proteases. This protein is a secreted enzyme that is proposed to regulate the availability of insulin like growth factors (IGFs) by cleaving IGF binding proteins. It has also been suggested to be a regulator of cell growth. Variations in the promoter region of this gene are the cause of susceptibility to age related macular degeneration type 7.