Nectin 1 Polyclonal Antibody, 50ul Pasteur Pipets Mutations in PEX2 result in

Mutations in PEX2 result in one form of Zellweger syndrome and infantile Refsum disease

The edge of the wells protrude to prevent cross-contamination and to facilitate sealing

Mutations in this gene are associated with mandibulofacial dysostosis with microcephaly

The protein is an in vivo substrate of matrix metalloproteinase 2

Nectin 1 Polyclonal Antibody, 50ul Pasteur Pipets Mutations in PEX2 result inNECTIN1 encodes nectin cell adhesion molecule 1 that plays a role in the organization of adherens junctions and tight junctions in epithelial and endothelial cells. The protein is a calcium(2+) independent cell cell adhesion molecule that belongs to the immunoglobulin superfamily and has 3 extracellular immunoglobulin like loops, a single transmembrane domain (in some isoforms), and a cytoplasmic region. This protein acts as a receptor for