IIGP5 Polyclonal Antibody, 100ul Cell Screening and Imaging Evidence indicates that mutations in

Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1)

F7 encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis

APOBEC3A is a member of the cytidine deaminase gene family

Interleukin 17A and its receptor play a pathogenic role in many inflammatory and autoimmune diseases such as rheumatoid arthritis

Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported

IIGP5 Polyclonal Antibody, 100ul Cell Screening and Imaging Evidence indicates that mutations inCatalytic activity: GTP + H(2)O = GDP + phosphate. Belongs to the interferon inducible GTPase family.