TRPM4 Rabbit Polyclonal Antibody, 20ul Antibody Humanization Mutations of this gene are

Mutations of this gene are associated with Seckel syndrome

Mutations in this gene are a cause of aortic aneurysms and dissections

The encoded protein is thought to have essential roles in organization of the actin cytoskeleton and in cell polarity

MRPL9 is a nuclear gene encoding 39S ribosomal protein L9 mitochondrial component of the 39S subunit of the mitochondrial ribosome

TRPM4 Rabbit Polyclonal Antibody, 20ul Antibody Humanization Mutations of this gene areThe protein encoded by this gene is a calcium activated nonselective ion channel that mediates transport of monovalent cations across membranes thereby depolarizing the membrane. The activity of the encoded protein increases with increasing intracellular calcium concentration but this channel does not transport calcium.