SSA27 Polyclonal Antibody, 20ul Metabolic enzymes tool compounds Mutations in this gene cause

Mutations in this gene cause lissencephaly 4

Carboxy-terminal modifications and differences in subcellular localization allow these three proteins to respond to and act on distinct signaling molecules

This protein has been shown to function in part through the regulation of intracellular Ca2+ mobilization

a novel family that is similar to the chemokine and the transmembrane 4 superfamilies of signaling molecules

Both proteins contain a NAD+ binding domain similar to NAD+-dependent 2-hydroxyacid dehydrogenases

SSA27 Polyclonal Antibody, 20ul Metabolic enzymes tool compounds Mutations in this gene causeThis antigen is recognized by a subset of anti centromere antibodies from patients with scleroderma and or Sjogren's syndrome. Subcellular localization has not yet been established.