mtDNA Sequencing


The diagnosis of mitochondrial disorders is challenging because of the clinical variability and genetic heterogeneity. Mitochondrial sequencing with NGS technologies provides a robust high-throughput platform for comprehensive detection and analysis of mitochondrial mutations.

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NGSMT-LP mtDNA Sequencing Please inquire



MCLAB offers mtDNA enrichment method and library construction for: 1. Detection of mitochondrial point mutations and deletions; 2. Rapid analysis of mtDNA; 3. Accurate and sensitive measurement of heteroplasmy

Sample Requirements:

Miminal 0.5ug gDNA at high quality and purity, without contaminants of ssDNA, RNA, oligos, organic contaminants such as phenol and ethanol, does not contain more than 1 mM EDTA

Shipping Conditionx:

On dry ice through FedEx overnight

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mtDNA Sequencing, mtDNA Sequencing

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