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Milne LM, Kyi MS, Chiodini PL, Warhurst DC. Accuracy of routine laboratory diagnosis of malaria in the United Kingdom. J Clin Pathol. 1994;47:740–2. The above one is a cute minion printable you might love getting framed and decorating your bedroom with. Get this cute wall art printable HERE . A Lot Of Minion Figurines Are Classy! Image Source M. Goto, E. Honda, A. Ogura, A. Nomoto and K.-I. Hanaki, BioTechniques, 2009, 46, 167–172 CrossRef CAS PubMed. Patel JC, Lucchi NW, Srivastava P, Lin JT, Sug-Aram R, Aruncharus S, et al. Field evaluation of a real-time fluorescence loop-mediated isothermal amplification assay, RealAmp, for the diagnosis of malaria in Thailand and India. J Infect Dis. 2014;210:1180–7. L. A. Rigano, M. R. Marano, A. P. Castagnaro, A. M. Do Amaral and A. A. Vojnov, BMC Microbiol., 2010, 10, 176 CrossRef.
Y. Zhou, J. Xiao, X. Ma, Q. Wang and Y. Zhang, Appl. Microbiol. Biotechnol., 2018, 102, 5299–5308 CrossRef CAS PubMed. T. Iwamoto, T. Sonobe and K. Hayashi, J. Clin. Microbiol., 2003, 41, 2616–2622 CrossRef CAS PubMed. J. Yamagishi, L. R. Runtuwene, K. Hayashida, A. E. Mongan, L. A. N. Thi, L. N. Thuy, C. N. Nhat, K. Limkittikul, C. Sirivichayakul, N. Sathirapongsasuti, M. Frith, W. Makalowski, Y. Eshita, S. Sugano and Y. Suzuki, Sci. Rep., 2017, 7, 3510 CrossRef.
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K. Imai, N. Tarumoto, K. Amo, M. Takahashi, N. Sakamoto, A. Kosaka, Y. Kato, K. Mikita, J. Sakai, T. Murakami, Y. Suzuki, S. Maesaki and T. Maeda, Parasitol. Int., 2018, 67, 34–37 CrossRef CAS. S. Roy, S. X. Wei, J. L. Z. Ying, M. Safavieh and M. U. Ahmed, Biosens. Bioelectron., 2016, 86, 346–352 CrossRef CAS PubMed. D. Mabey, R. W. Peeling, A. Ustianowski and M. D. Perkins, Nat. Rev. Microbiol., 2004, 2, 231–240 CrossRef CAS.
Now that your kids (or you) are die-hard minion fans, why not cram the room with minions to the brim? Kyabayinze DJ, Zongo I, Cunningham J, Gatton M, Angutoko P, Ategeka J, et al. HRP2 and pLDH-based rapid diagnostic tests, expert microscopy, and PCR for detection of malaria infection during pregnancy and at delivery in areas of varied transmission: a prospective cohort study in Burkina Faso and Uganda. PLoS One. 2016;11:e0156954. The reactions were performed using a Loopamp DNA Amplification Reagent Kit (Eiken Chemical). Detection of the LAMP amplicons was performed by real-time measurements of turbidity using a Loopamp real-time turbidimeter LA-200 (Eiken Chemical) and visual observations of the colour changes with the naked eye under natural light. The final reaction volume was 25 μL, comprising 40 pmol of the FIP primer and 40 pmol of the BIP primer, 20 pmol of each loop primer, 5 pmol of F3 and B3 primers, 1 μL of the Bst DNA polymerase, reaction buffer (20 mM Tris–HCl, 10 mM KCl, 8 mM MgSO 4, 10 mM (NH 4) 2SO 4, 0.1% Tween 20, 0.8 M betaine, and 1.4 mM each dNTP), and 1 μL of plasmid DNA or 8 μL of genomic DNA samples. Reactions were carried out at 62, 63, 64, and 65 °C in duplicate to find the optimum temperature for the LAMP amplification. The detection limit and specificity of the LAMP assay D. Zhang, J. Jiang, J. Chen, Q. Zhang, Y. Lu, Y. Yao, S. Li, G. Logan Liu and Q. Liu, Biosens. Bioelectron., 2015, 70, 81–88 CrossRef CAS PubMed.Cheng Q, Cunningham J, Gatton ML. Systematic review of sub-microscopic P. vivax infections: prevalence and determining factors. PLoS Negl Trop Dis. 2015;9:e3413. Hu SF, Li M, Zhong LL, Lu SM, Liu ZX, Pu JY, et al. Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection and differentiation of dengue virus serotypes 1-4. BMC Microbiol. 2015;15:265. Commercially available quartz crystals enclosed by electrodes and custom-made QCM system for LAMP and readout 153 N. Nakamura, K. Ito, M. Takahashi, S. Hongo, K. Hashimoto, M. Kawamoto, A. Taniguchi, N. Kamatani and N. Gemma, Clin. Biochem., 2009, 42, 1158–1161 CrossRef CAS. CLIA Categorizations, available at: https://www.fda.gov/medical-devices/ivd-regulatory-assistance/clia-categorizations.
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