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ABSTRACT: Aim
To design a novel method to rapidly detect the quantitative alteration of mtRNA in patients with tumors.Methods
Oligo 6.22 and Primer Premier 5.0 bio-soft were used to design 15 pairs of primers of mtRNA cDNA probes in light of the functional and structural property of mtDNA, and then RT-PCR amplification was used to produce 15 probes of mtRNA from one normal gastric mucosal tissue. Total RNA extracted from 9 gastric cancers and corresponding normal gastric mucosal tissues was reverse transcribed into cDNA labeled with fluorescein. The spotted mtDNA microarrays were made and hybridized. Finally, the microarrays were scanned with a GeneTAC laser scanner to get the hybridized results. Northern blot was used to confirm the microarray results.Results
The hybridized
SUBMITTER: Han CB
PROVIDER: S-EPMC4205380 | biostudies-literature | 2005 Jan
REPOSITORIES: biostudies-literature