mtDNA Sequencing
$0.00
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.
| SKU | OPTIONS | Price | Quantity | ||
|---|---|---|---|---|---|
| NGSMT-LP | mtDNA Sequencing | Please inquire |
- Description
- Additional information
- Documents
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Description
Description:
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
Additional information
| OPTIONS | mtDNA Sequencing, mtDNA Sequencing |
|---|
There is no documents for this product.Will be available soon.
The Q&A for this product will be available soon.
