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Molecular procedures to amplify, clone and sequence these genes are described elsewhere [41].
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Whole genome amplification (WGA) is an in vitro procedure to amplify a genomic DNA (gDNA) sample to generate amplified DNA (wgaDNA) for further molecular genetic analyses, and has been considered by some as a potential solution to the problem of limiting gDNA availability.
The labeling was performed using Eberwine procedure to amplify the starting material.
We modified the well-established neurosphere procedure to amplify the PRPs of the postnatal SVZ.
An enrichment step was performed on samples that were negative by DAL procedure to amplify the number of coliphage in the samples.
We used this procedure to amplify the genomes of 37 single cells from sections of frozen mouse tumor and normal lung tissues, which were micro-dissected and catapulted onto micro-tube caps.
Standard PCR procedures were used to amplify each region from genomic DNA from single male flies.
Standard polymerase chain reaction (PCR) procedures were used to amplify each region from genomic DNA from single male flies.
The PCR procedure was able to amplify the 0.7-kb B. cinerea fragment form mixed samples of DNA as low as 2 pg B. cinerea genomic DNA and 1 μg plant DNA.
This procedure allowed us to amplify the strength of the searched signal.
This procedure was used to amplify a specific fragment of the NS5 gene within the flavivirus genome.
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