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19081“…CONCLUSION: Real-time quantitative PCR using specific primers and molecular beacon probes for the selected amplicon described in this study can detect three tick-borne pathogens simultaneously in an accurate manner.…”
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19082por Abera, Tsegalem, Thangavelu, Ardhanary, Joy Chandran, Navamani Daniel, Raja, Angamuthu“…Thus, the objective of present study was to develop highly sensitive N gene target SYBR Green I real time RT-PCR for specific detection and quantification of PPRV in clinical samples. A set of primers was designed to detect the nucleocapsid (N) gene of PPRV. …”
Publicado 2014
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19083por Villano, Gianmarco, Turato, Cristian, Quarta, Santina, Ruvoletto, Mariagrazia, Ciscato, Francesco, Terrin, Liliana, Semeraro, Rossella, Paternostro, Claudia, Parola, Maurizio, Alvaro, Domenico, Bernardi, Paolo, Gatta, Angelo, Pontisso, Patrizia“…Liver cDNA was amplified using specific primers for mouse-homologous SerpinB3 isoforms and automatically sequenced. …”
Publicado 2014
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19084por Evans, Christian C., LePard, Kathy J., Kwak, Jeff W., Stancukas, Mary C., Laskowski, Samantha, Dougherty, Joseph, Moulton, Laura, Glawe, Adam, Wang, Yunwei, Leone, Vanessa, Antonopoulos, Dionysios A., Smith, Dan, Chang, Eugene B., Ciancio, Mae J.“…DNA was subjected both to quantitative PCR using primers specific to the 16S rRNA encoding genes for Bacteroidetes and Firmicutes and to sequencing for lower taxonomic identification using the Illumina MiSeq platform. …”
Publicado 2014
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19085por Selvi, Nur, Kosova, Buket, Hekimgil, Mine, Gündüz, Cumhur, Kaymaz, Burçin Tezcanlı, Karaca, Emin, Saydam, Güray, Tombuloğlu, Murat, Büyükkeçeci, Filiz, Çağırgan, Seçkin, Ertan, Yeşim, Topçuoğlu, Nejat“…To identify the mcr breakpoint, real-time PCR was performed using specific primers and the FastStart DNAMaster SYBR Green I Kit. …”
Publicado 2012
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19086por Armingohar, Zahra, Jørgensen, Jørgen J., Kristoffersen, Anne Karin, Abesha-Belay, Emnet, Olsen, Ingar“…The V3-V5 region of the 16S rDNA (V3-V5) was polymerase chain reaction (PCR)-amplified, and the amplicons were cloned into Escherichia coli, sequenced, and classified (GenBank and the Human Oral Microbiome database). Species-specific primers were used for the detection of Porphyromonas gingivalis. …”
Publicado 2014
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19087por Bazzocchi, Chiara, Mariconti, Mara, Sassera, Davide, Rinaldi, Laura, Martin, Elena, Cringoli, Giuseppe, Urbanelli, Sandra, Genchi, Claudio, Bandi, Claudio, Epis, Sara“…DNAs were extracted, and amplified using 16S ribosomal RNA primers conserved in the Midichloria genus. Furthermore, sera from dogs exposed to the risk of tick bite were analyzed in order to evaluate the presence of antibodies against the recombinant flagellar protein (rFliD) from M. mitochondrii using an ELISA test. …”
Publicado 2013
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19088por Freitas, Luciana Bueno, Chen, Zigui, Muqui, Elaine Freire, Boldrini, Neide Aparecida Tosato, Miranda, Angélica Espinosa, Spano, Liliana Cruz, Burk, Robert D.“…The DNA was isolated using QIAamp DNA Mini Kit and HPV was detected by amplification with PGMY09/11 primers and positive samples were genotyped by RFLP analyses and reverse line blot. …”
Publicado 2014
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19089por Chen, Qingliang, Shi, Xiaolu, Li, Yinghui, Jiang, Yixiang, Lin, Yiman, Qiu, Yaqun, Li, Qingge, Hu, Qinghua“…METHODS: In this study, specific primers and modified molecular beacon probes of nine specific virulence genes, whose 5′end were added with homo tail sequence, were designed; and a two-tube modified molecular beacon based multiplex real–time PCR (rtPCR) assay for the identification of five Escherichia coli pathotypes, including ETEC, EAEC, EPEC, EHEC and EIEC was developed and optimized. …”
Publicado 2014
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19090por Snelling, Timothy J., Genç, Buğra, McKain, Nest, Watson, Mick, Waters, Sinéad M., Creevey, Christopher J., Wallace, R. John“…Sanger sequenced 1.3 kb 16S rRNA gene amplicons identified the main species of Methanobrevibacter present to be a SGMT Clade member Mbb. millerae (≥91% of OTUs); Methanosphaera comprised the remainder of the OTUs. The primers did not amplify ruminal Thermoplasmatales-related 16S rRNA genes. …”
Publicado 2014
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19091por Lam, Connie, Octavia, Sophie, Sintchenko, Vitali, Gilbert, Gwendolyn L, Lan, Ruiting“…This study used microarray data to identify and select a panel of RDs; primers and probes for these RDs were then designed to test for the presence or absence of these regions in a novel and less expensive multiplex PCR-based reverse line blot (mPCR/RLB) assay. …”
Publicado 2014
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19092por Waggoner, Jesse J., Balassiano, Ilana, Abeynayake, Janaki, Sahoo, Malaya K., Mohamed-Hadley, Alisha, Liu, Yuanyuan, Vital-Brazil, Juliana Magalhães, Pinsky, Benjamin A.“…METHODOLOGY/PRINCIPAL FINDINGS: For the pathogenic rtPCR, a new hydrolysis probe was designed for use with primers from the UFI assay, which targets the 16S gene. …”
Publicado 2014
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19093por Choi, Igseo, Bao, Hua, Kommadath, Arun, Hosseini, Afshin, Sun, Xu, Meng, Yan, Stothard, Paul, Plastow, Graham S, Tuggle, Christopher K, Reecy, James M, Fritz-Waters, Eric, Abrams, Samuel M, Lunney, Joan K, Guan, Le Luo“…CONCLUSIONS: Our porcine specific GR primers and protocol minimize the number of reads of globin transcripts in whole blood samples and provides increased coverage as well as accuracy and reproducibility of transcriptome analysis. …”
Publicado 2014
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19094por LOU, XIAOLI, HOU, YANQIANG, LIANG, DONGYU, PENG, LIANG, CHEN, HONGWEI, MA, SHANYUAN, ZHANG, LURONG“…Standard Alu-puc57 vectors were constructed and 5 pairs of specific primers were designed. Valuation was conducted concerning linearity, variation and recovery. …”
Publicado 2015
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19095por Shaukat, Shahzad, Angez, Mehar, Alam, Muhammad Masroor, Jebbink, Maarten F, Deijs, Martin, Canuti, Marta, Sharif, Salmaan, de Vries, Michel, Khurshid, Adnan, Mahmood, Tariq, van der Hoek, Lia, Zaidi, Syed Sohail Zahoor“…To further characterize the viruses, VIDISCA-positive samples were amplified and sequenced with gene specific primers. RESULTS: Simplified VIDISCA detected seven viruses (70%) and the proportion of eukaryotic viral sequences from each sample ranged from 8.3 to 45.8%. …”
Publicado 2014
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19096por Li, Ximei, Gao, Wenhui, Guo, Huanle, Zhang, Xianlong, Fang, David D, Lin, Zhongxu“…On the other hand, the developmental efficiency of markers and polymorphism of designed primers are comparatively low. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-1046) contains supplementary material, which is available to authorized users.…”
Publicado 2014
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19097por Méndez-Martínez, Rocío, Rivera-Martínez, Norma E, Crabtree-Ramírez, Brenda, Sierra-Madero, Juan G, Caro-Vega, Yanink, Galván, Silvia C, de León, David Cantú, García-Carrancá, Alejandro“…METHODS: In the present study we determined the prevalence and nature of HPV co-infections in the anal canal of 324 HIV+ MSM attending a high specialty medical center in Mexico City, DNA extraction and amplification with generic primers for HPV was performed, followed by detection of specific types and co-infections with INNO-Lipa, and identification of variants by amplification and sequencing of the E6 and LCR region of HPV 16. …”
Publicado 2014
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19098por Lee, Ping Chin, Chong, Eric Tzyy Jiann, Anderios, Fread, AL Lim, Yvonne, Chew, Ching Hoong, Chua, Kek Heng“…Discordance results between two PCR assays were further confirmed by sequencing using 18S ssu rRNA species-specific primers. RESULTS: Of the 207 malaria samples, Plasmodium knowlesi (73.4% vs 72.0%) was the most prevalent species based on two PCR assays, followed by Plasmodium falciparum (15.9% vs 17.9%), and Plasmodium vivax (9.7% vs 7.7%), respectively. …”
Publicado 2015
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19099por Azizi, Omid, Shakibaie, Mohammad Reza, Modarresi, Farzan, Shahcheraghi, Fereshteh“…The presence of bla(OXA) genes among the isolates were studied by duplex-polymerase chain reaction and application of appropriate primers. Biofilm formation was detected by microtiter plate method. …”
Publicado 2015
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19100“…Phytophthora specific real-time PCR assay was developed using specific primers based on internal transcribed spacer (ITS) 1 and 2. …”
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