Trypsin-3 Polyclonal Antibody, 50ul Antisense Oligonucleotides |disease:Defects in CFD are the

|disease:Defects in CFD are the cause of complement factor D deficiency

This gene encodes a protein that belongs to a family of helicases that are involved in the ATP-dependent unwinding of nucleic acid duplexes

|Belongs to the IFI6/IFI27 family

The isoform encoded by the unspliced mRNA

Trypsin-3 Polyclonal Antibody, 50ul Antisense Oligonucleotides |disease:Defects in CFD are thePRSS3 encodes a trypsinogen, which is a member of the trypsin family of serine proteases. This enzyme is expressed in the brain and pancreas and is resistant to common trypsin inhibitors. It is active on peptide linkages involving the carboxyl group of lysine or arginine. This gene is localized to the locus of T cell receptor beta variable orphans on chromosome 9. Four transcript variants encoding different isoforms have been described for this gene.