MST4 Polyclonal Antibody, 20ul Cell Culture & Maintenance a S1 motif domain and

a S1 motif domain and exists as two alternatively spliced isoforms that map to human chromosome 1p35

Defects in this gene can result in X-linked creatine deficiency syndrome

where carcinogen-induced damage can lead to translocations and aberrant transcripts of this gene

Individual preparations of the Mediator complex lacking one or more distinct subunits have been variously termed ARC

and nucleates formation of a stable preinitiation complex

MST4 Polyclonal Antibody, 20ul Cell Culture & Maintenance a S1 motif domain andThe product of this gene is a member of the GCK group III family of kinases, which are a subset of the Ste20 like kinases. The encoded protein contains an amino terminal kinase domain, and a carboxy terminal regulatory domain that mediates homodimerization. The protein kinase localizes to the Golgi apparatus and is specifically activated by binding to the Golgi matrix protein GM130. It is also cleaved by caspase 3 in vitro, and may function in the