Stat1 Polyclonal Antibody, 100ul[BT-AP08613] Immuno Plates Defects in this gene are

Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis

Defects in this gene are a cause of familial amyloidosis Finnish type (FAF)

This protein localizes to the mitochondrial inner membrane

coli and yeast cells

A related pseudogene is located near this gene

Stat1 Polyclonal Antibody, 100ul[BT-AP08613] Immuno Plates Defects in this gene areSignal transducer and activator of transcription 1 alpha beta encoded by STAT1 is a member of the STAT protein family. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homodimers.