MTDNA PLUS® NGS SEQUENCING & LIBRARY PREPARATION KIT
-Mitochondrial diseases form part of genetic diseases.
- The mutations in this particular DNA in mitochondria, the most important organ in the cell's energy metabolism, cause mitochondrial diseases such as Leber's hereditary optic atrophy (LHON), Kearn Sayre Syndrome (CSS), Leigh syndrome, Narp syndrome, Melas and MERRF.
- This kit enables rapid and reliable diagnosis of these diseases.
- It is compatible with illuminina (Miseq, MiSeq, HiSeq, NextSeq 550).