ZPI Polyclonal Antibody, 100ul Erlenmeyer Flasks Mutations in this gene cause

Mutations in this gene cause nocturnal frontal lobe epilepsy type 1

Family members are characterized by two N-terminal F-spondin domains (FS1 and FS2)

Isoform 1 has lower affinity for DNA

Mitogen-activated protein kinase kinase kinase kinase 3 activates key effectors in cell signalling

lymph nodes

ZPI Polyclonal Antibody, 100ul Erlenmeyer Flasks Mutations in this gene causeThe protein encoded by this gene belongs to the serpin family. It is predominantly expressed in the liver and secreted in plasma. It inhibits the activity of coagulation factors Xa and XIa in the presence of protein Z, calcium and phospholipid. Mutations in this gene are associated with venous thrombosis. Alternatively spliced transcript variants have been found for this gene.