SYT4 Polyclonal Antibody, 20ul Polyclonal Antibodies Additional transcript variants have been

Additional transcript variants have been described but their full-length nature is not known

which subsequently combine as a tetramer to produce haptoglobin

Mutations in MBTPS2 have been associated with ichthyosis follicularis with atrichia and photophobia (IFAP syndrome)

Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3)

SYT4 Polyclonal Antibody, 20ul Polyclonal Antibodies Additional transcript variants have beencofactor: 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 2 C2 domains.,tissue specificity: Expressed in brain. Within brain, expression is highest in hippocampus, with