DBP Polyclonal Antibody, 20ul Stepper Mutations in C9 cause component

Mutations in C9 cause component C9 deficiency

Dysregulation of this gene has been associated with the growth and progression of certain cancers

and the protein is the target for neurodegeneration induced by organophosphorus compounds and chemical warfare agents

The encoded protein (caspase 2) may function in stress-induced cell death pathways

DBP Polyclonal Antibody, 20ul Stepper Mutations in C9 cause componentThe protein encoded by this gene belongs to the albumin gene family. It is a multifunctional protein found in plasma, ascitic fluid, cerebrospinal fluid and on the surface of many cell types. It binds to vitamin D and its plasma metabolites and transports them to target tissues. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.