Examples of PCR amplification with three individual polymorphic Alu-containing loci (MLS 19, MLS 50 and MLS 65) in ten tracer (lines t1–t10) and one driver (line Dr) DNA samples

<p><b>Copyright information:</b></p><p>Taken from "Whole-genome experimental identification of insertion/deletion polymorphisms of interspersed repeats by a new general approach"</p><p>Nucleic Acids Research 2005;33(2):e16-e16.</p><p>Published online 26 Jan 2005</p><p>PMCID:PMC548376.</p><p>© The Author 2005. Published by Oxford University Press. All rights reserved</p> Lines K+ and K− represent positive and negative controls, respectively. M, DNA fragments of a 100 bp ladder length marker (SybEnzime). Gray and white arrows to the left of the electrophoregrams indicate the predicted locations of the Alu containing and Alu-free PCR products, respectively. Scheme of genomic primers location is represented at the bottom