SLC9A9 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.

NHE-9 Polyclonal Antibody detects endogenous levels of NHE-9 protein.

Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB: 1:500-1:2000, ELISA: 1:40000. Not yet tested in other applications.

NHE-9 Polyclonal Antibody product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Find more details at http://www.abbkine.com/product/nhe-9-polyclonal-antibody-abp51962.