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| Teaching Since: | Apr 2017 |
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| Questions Answered: | 12843 |
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MBA, Ph.D in Management
Harvard university
Feb-1997 - Aug-2003
Professor
Strayer University
Jan-2007 - Present
We need to know how much DNA has been extracted prior to amplifying the 15 loci of interest. A technique called quantitative real-time polymerase chain reaction (qRT-PCR) is available to help us. Please explain how this works and why an internal standard is included in each reaction. Please touch on the why you need to make a standard curve with each quantification run.
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