TRPM4 Rabbit Polyclonal Antibody, 20ul Antibody Humanization an OPR domain and a

an OPR domain and a semi-Cdc42/Rac interactive binding (CRIB) domain

Mutations of this gene are associated with Seckel syndrome

and like the mouse gene

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 an OPR domain and aThe 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.