SLC9A1 (Solute Carrier Family 9 Member A1) is a Protein Coding gene. Diseases associated with SLC9A1 include Lichtenstein-Knorr Syndrome and Myocardial Stunning. Among its related pathways are Glycosaminoglycan metabolism and Metabolism. SLC9A1 encodes a Na+/H+ antiporter that is a member of the solute carrier family 9. The encoded protein is a plasma membrane transporter that is expressed in the kidney and intestine. This protein plays a central role in regulating pH homeostasis, cell migration and cell volume. This protein may also be involved in tumor growth.
Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000 ELISA 1:5000-20000.
SL9A1 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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