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Mitochondrial Disease Research

Mitochondrial Disease Research

Determining Mitochondrial Gene Mutation Phenotypes

Mitochondrial diseases are a defined group of disorders that are a result of a dysfunctional mitochondrial respiratory chain. Genetic mutations are the cause of numerous metabolic diseases and disorders, including both rare and well-documented. This group of diseases can affect a single organ, as well as multiple organ systems. Researchers are using Agilent Seahorse XF technology to gain unique and powerful insights into these diseases.

Learn more about How XF Technology Works

Click to search either the Seahorse XF Publications Database or the Seahorse Cell Reference Database

For Research Use Only. Not for use in diagnostic procedures.