New special offers are available!
mtDNA Sequencing
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.

Click To Find Out Price

Name Cat# Description Price Qty
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

There is no documents for this product.Will be available soon.
The Q&A for this product will be available soon.
T4 Endonuclease VII
Customized Competent <i>E. coli</i>
BL21(DE3) Competent <i>E. coli</i>
T4 Endonuclease VII Customized Competent E. coli BL21(DE3) Competent E. coli
HB101 Competent <i>E. coli</i>
BL21(DE3)pLysS Competent <i>E. coli</i>
Dh5-Alpha Competent  <em>E. coli </em>
HB101 Competent E. coli BL21(DE3)pLysS Competent E. coli Dh5-Alpha Competent E. coli
Exonuclease I (<i>E. coli</i>)
<em>Taq</em> DNA Polymerase
Brij-35 (30% Solution)
Exonuclease I (E. coli) Taq DNA Polymerase Brij-35 (30% Solution)