Trypsin-1 Polyclonal Antibody, 100ul Peptide Synthesis During catalysis

During catalysis

and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype

and expansion of this repeat from the normal 6 copies to 8-13 copies leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease

|disease:Defects in ACAN are the cause of spondyloepiphyseal dysplasia type Kimberley (SEDK)

Trypsin-1 Polyclonal Antibody, 100ul Peptide Synthesis During catalysisPRSS1 encodes a trypsinogen, which is a member of the trypsin family of serine proteases. This enzyme is secreted by the pancreas and cleaved to its active form in the small intestine. It is active on peptide linkages involving the carboxyl group of lysine or arginine. Mutations in this gene are associated with hereditary pancreatitis. This gene and several other trypsinogen genes are localized to the T cell receptor beta locus on chromosome 7.