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25 ng of DNA diluted in 10 1 TE buffer were amplified for each PCR reaction.
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The corresponding specific DNA products were amplified for each pathogen.
PCR products were amplified for 33 cycles.
Libraries were amplified for 16 18 cycles.
Sequences were amplified for 30 cycles.
Cells were rinsed with 1 × TBS and signal was amplified for 5 min in the amplification buffer (1 : 200 diluted biotinyl-tyramine, 0.01% hydrogen peroxide diluted in 100 mM Tris-HCl, pH 8.0).
This is amplified for those who work part-time.
These challenges are amplified for enabling technologies, which are the central focus of this article.
A yeast GAPDH fragment was amplified for normalization.
Genomic DNA was amplified for 40 cycles.
The cDNA was amplified for 28 cycles.
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