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. 2014 Aug 1;5:395. doi: 10.3389/fmicb.2014.00395

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Copyright © 2014 Chander, Koelbl, Puckett, Moser, Klingele, Liles, Carrias, Mead and Schoenfeld.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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RT-LAMP using OmniAmp polymerase for detection of RNA targets: West Nile virus (WNV), Crimean-Congo hemorrhagic virus (CCHF), Ebola virus (EBoV), Swine influenza virus (SIV), MS2, and Bovine viral diarrhea virus (BVDV). (A) For each pathogen, 10-fold serial dilutions of extracted RNA were prepared in water and used as template in LAMP reaction. Results are averages of three TTR values for each dilution. (No amplification is indicated by “^**”). (B) MS2 LAMP products were separated on 2% agarose gel.