KCNJ8 (Potassium Voltage-Gated Channel Subfamily J Member 8) is a Protein Coding gene. Diseases associated with KCNJ8 include Hypertrichotic Osteochondrodysplasia and Sudden Infant Death Syndrome. Among its related pathways are Inwardly rectifying K+ channels and Antiarrhythmic Pathway, Pharmacodynamics.
Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000 ELISA 1:5000-20000.
IRK8 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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