Primary coenzyme Q (CoQ) deficiency causes a heterogeneus group of mitochondrial diseases with high variability in severity and tissues affectation. It has been identified that ADCK2 gene is involved in CoQ10 biosynthesis and its mutation is responsible of a mitochondrial myopathy and liver dysfunction in humans.
应用类型
WB
免疫原
Synthetic peptide, corresponding to amino acids 226-286 of Human ADCK2.
