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NHE-9 Polyclonal Antibody, 100ul Petri Dishes Mutations in this gene are

SKU: 50945150671

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NHE-9 Polyclonal Antibody, 100ul Petri Dishes Mutations in this gene areSLC9A9 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.

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Description

Mutations in this gene are associated with primary autosomal recessive microcephaly

and cell-cycle progression

This gene encodes a possible magnesium transporter

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

NHE-9 Polyclonal Antibody, 100ul Petri Dishes Mutations in this gene areSLC9A9 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.

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