Tag/hybridization-based sensitive detection of polymerase chain reaction products.

Anal Biochem

Future Technology Management Center, Corporate R&D, NGK Insulators, Mizuho, Nagoya 467-8530, Japan; Graduate School of Biomedical Engineering, Tohoku University, Aoba, Sendai 980-8579, Japan.

Published: November 2014

The polymerase chain reaction (PCR) is an important technology to amplify a single copy or a few copies of DNA segment in genomic DNAs, visualizing the segment as DNA fragment. Thus, PCR is frequently used in various examinations such as detection of bacteria and fungi in the food industry. Here, we report a simple and sensitive method for detection of PCR products using single-strand tag sequence and hybridization of the tag sequence to the complementary tag sequence immobilized on solid material (STH). The detection sensitivity was found to be at least 50 times higher than electrophoresis/ethidium bromide (EtBr) visualization for approximately a 500-bp fragment and higher than the ordinary hybridization, that is, hybridization of denatured PCR product to probe sequence immobilized on solid material.

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Source
http://dx.doi.org/10.1016/j.ab.2014.07.010DOI Listing

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