SLC9A5 (Solute Carrier Family 9 Member A5) is a Protein Coding gene. Diseases associated with SLC9A5 include Familial Paroxysmal Kinesigenic Dyskinesia and Episodic Kinesigenic Dyskinesia 1. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and ADP signalling through P2Y purinoceptor 12.
Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000 ELISA 1:5000-20000.
SL9A5 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.
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