NHE-9 Polyclonal Antibody, 100ul Petri Dishes This gene encodes a possible

This gene encodes a possible magnesium transporter

and cell-cycle progression

This powerful solution offers 200 rxns per bottle at 1 rxn/μl

Mutations in this gene are associated with primary autosomal recessive microcephaly

and peptides to more complex organic molecules

NHE-9 Polyclonal Antibody, 100ul Petri Dishes This gene encodes a possibleSLC9A9 encodes a sodium proton exchanger that is a member of the solute carrier 9 protein family. Solute carrier family 9 member A9 localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in SLC9A9 are associated with autism susceptibility 16 and attention deficit hyperactivity disorder.