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 Cell Analysis technology to gain unique and powerful insights into these diseases.
Learn more about How Seahorse XF Technology Works
Learn more about MitoXpress & pH-Xtra Products
Search scientific publications that reference and/or cite Agilent Cell Analysis products.
For Research Use Only. Not for use in diagnostic procedures.