A Novel Universal Primer-Multiplex-PCR Method with Sequencing Gel Electrophoresis Analysis

<div><p>In this study, a novel <u>u</u>niversal <u>p</u>rimer-<u>m</u>ultiplex-PCR (UP-M-PCR) method adding a <u>u</u>niversal <u>p</u>rimer (UP) in the multiplex PCR reaction system was described. A universal adapter was designed in the 5′-end of each specific primer pairs which matched with the specific DNA sequences for each template and also used as the <u>u</u>niversal <u>p</u>rimer (UP). PCR products were analyzed on <u>s</u>equencing <u>g</u>el <u>e</u>lectrophoresis (SGE) which had the advantage of exhibiting extraordinary resolution. This method overcame the disadvantages rooted deeply in conventional multiplex PCR such as complex manipulation, lower sensitivity, self-inhibition and amplification disparity resulting from different primers, and it got a high specificity and had a low detection limit of 0.1 ng for single kind of crops when screening the presence of genetically modified (GM) crops in mixture samples. The novel developed multiplex PCR assay with sequencing gel electrophoresis analysis will be useful in many fields, such as verifying the GM status of a sample irrespective of the crop and GM trait and so on.</p>