Trypsin-1 Polyclonal Antibody, 100ul Peptide Synthesis In normal tissues

In normal tissues

AMBRA1 (Activating molecule in BECN1-regulated autophagy protein 1)

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

family members have a proline-rich domain that binds SH3 and WW domain-containing proteins

leukocyte elastase

Trypsin-1 Polyclonal Antibody, 100ul Peptide Synthesis In normal tissuesPRSS1 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.