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The layers of repetitive elements added to genomic DNA by genetic drift can account for fluctuations in the amounts of the non-coding genomic DNA in different species.
Compatible results were obtained with the measurement of formal potential differences between mixed SAMs and target DNA (complementary and non-complementary DNA) in different target DNA concentrations.
In September, the National Institutes of Health began a $190 million program to start mapping epigenetic marks on DNA in different tissues.
But new experiments show that protons and photons damage DNA in different ways.
To contrast the effects of metal ions on the conductive ability of DNA in different condition, we measured I V curves of DNA at different Ni2+ concentrations in alkaline environment.
The BB.fw and BB.rv primer set were subsequently optimized to be used in real time quantitative PCR assays and allowed to accurately quantify B. bassiana DNA in different plant DNA backgrounds (leaves and seeds) without losing accuracy and efficiency.
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We also found the nucleolar organizer region (NOR), composed of ribosomal DNA (rDNA), in different locations.
To demonstrate this, we tested samples of known amounts of DNA targets in different ratios as well as genomic DNAs in different concentration ratios.
We designed specific primer pairs to detect the ChIP-DNA in different regions at the FLO11 promoter).
Therefore, in contrast to previous reports testing simultaneously mt-DNA and n-DNA in different conditions [ 20- 22], our data indicate that measurement of both markers is not necessary to increase the prognostic value.
Finally, artificial mixtures of genomic DNAs in different concentration ratios were tested.
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