SYT9 Polyclonal Antibody, 20ul Thermo Mix Mutations in PEX2 result in

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

Inhibits cell growth

The various isoforms have functional differences| with respect to ARF GAP activity and to G

The encoded protein primarily localizes to the centrosome

This gene belongs to the splicing factor SR family of genes

SYT9 Polyclonal Antibody, 20ul Thermo Mix Mutations in PEX2 result incofactor: Binds 3 calcium ions per subunit. The ions are bound to the C2 domains.,May be involved in Ca(2+) dependent exocytosis of secretory vesicles through Ca(2+) and phospholipid binding to the C2 domain or may serve as Ca(2+) sensors in the process of vesicular trafficking and exocytosis.,Belongs to the synaptotagmin family.,Contains 1 C2 domain.,Contains 2 C2 domains.,