Wansadaj JaroenramWansika KiatpathomchaiTimothy W. FlegelMahidol UniversityThailand National Center for Genetic Engineering and Biotechnology2018-09-132018-09-132009-04-01Molecular and Cellular Probes. Vol.23, No.2 (2009), 65-70089085082-s2.0-61449161963https://repository.li.mahidol.ac.th/handle/123456789/27253Loop-mediated isothermal amplification (LAMP) allows rapid amplification of nucleic acids under isothermal conditions using a set of four specifically designed primers that recognize six distinct target sequences. It can be combined with a chromatographic lateral flow dipstick (LFD) for highly specific, rapid and simple visual detection of WSSV-specific amplicons. Using this protocol, a 30-min amplification followed by 5 min hybridization with an FITC-labeled DNA probe and 5 min LFD resulted in visualization of DNA amplicons trapped at the LFD test line. Thus, 10 min for rapid DNA extraction followed by LAMP combined with LFD detection resulted in a total assay time of approximately 50 min. Detection sensitivity was comparable to other commonly-used methods for nested PCR detection of WSSV but had the additional advantages of reduced assay time, confirmation of amplicon identity by hybridization and elimination of electrophoresis with carcinogenic ethidium bromide. © 2008 Elsevier Ltd. All rights reserved.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyReviewSCOPUS10.1016/j.mcp.2008.12.003