REG1B Polyclonal Antibody, 100ul Mechanical Pipette Mutations in this gene are

Mutations in this gene are associated with congenital cataracts| facial dysmorphism and neuropathy syndrome (CCFDN)

This gene encodes a protein that belongs to the glutamate-gated ionic channel family

interacts with GRB2

Mutations in this gene result in alpha-2-plasmin inhibitor deficiency| which is characterized by severe hemorrhagic diathesis

REG1B Polyclonal Antibody, 100ul Mechanical Pipette Mutations in this gene areThis gene is a type I subclass member of the Reg gene family. The Reg gene family is a multigene family grouped into four subclasses, types I, II, III and IV based on the primary structures of the encoded proteins. This gene encodes a protein secreted by the exocrine pancreas that is highly similar to the REG1A protein. The related REG1A protein is associated with islet cell regeneration and diabetogenesis, and may be involved in pancreatic