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18881“…Molecular identification was performed using selective nifH-g1 primers. Alginate production and nitrogenase activity assay by each isolate of Azotobacter were carried out. …”
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18882por Husseiny, Mohamed I., Kuroda, Akio, Kaye, Alexander N., Nair, Indu, Kandeel, Fouad, Ferreri, Kevin“…Methylation-specific primers were designed to interrogate two or more CpG in the same assay. …”
Publicado 2012
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18883“…Based on GenBank sequence datasets of 115 rodent species, a 136 bp fragment of cytochrome b was selected as the most discriminatory mini-barcode, and rodent universal primers surrounding this fragment were designed. The efficacy of this new molecular tool was assessed on 946 samples including rodent tissues, feces, museum samples and feces/pellets from predators known to ingest rodents. …”
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18884por Wieben, Eric D., Aleff, Ross A., Tosakulwong, Nirubol, Butz, Malinda L., Highsmith, W. Edward, Edwards, Albert O., Baratz, Keith H.“…We tested for an association between an intronic TGC trinucleotide repeat in TCF4 and FECD by determining repeat length in 66 affected participants with severe FECD and 63 participants with normal corneas in a 3-stage discovery/replication/validation study. PCR primers flanking the TGC repeat were used to amplify leukocyte-derived genomic DNA. …”
Publicado 2012
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18885“…Intron based PCR was was used to amplify transcripts of PBMC pre-mRNA in which intron-5 had been removed (mRNA) while another set of primers was used to amplify intron 5-containing pre-transcripts (pre-mRNA). …”
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18886“…Odc1 genotyping was conducted using primers that amplify a 172-bp fragment containing the polymorphic base at +316. …”
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18887“…DNA was extracted from bacteria-infected and uninfected control cultures, and primers specific for Rickettsia 16S rRNA, ompB, and sca4 genes were used to generate PCR products that were subsequently sequenced. …”
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18888“…PCR amplification with primers directed outwards from the tet(S/M) gene identified the presence of a 4.3 kb circular form corresponding to the intervening chromosomal region between the two IS1216 elements, but lacking a replication origin. …”
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18889“…For qPCR-MN, infected MDCK-London cells in 96-well cell-culture plates are processed with minimal steps such that resulting samples are amenable to high-throughput analysis by downstream one-step quantitative reverse transcription PCR (qRT-PCR; SYBR Green chemistry with primers targeting a conserved region of the M1 gene of influenza A viruses). …”
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18890por Bhore, Subhash Janardhan, Amelia, Kassim, Wang, Edina, Priyadharsini, Sindhuja, Shah, Farida Habib“…To understand more about PvLCY-β and PvCHY-β, both strands of both cDNA clones were sequenced using M13 forward and reverse primers. Nucleotide and deduced protein sequences were analyzed and annotated using online bioinformatics tools. …”
Publicado 2013
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18891por Inanir, Ahmet, Tural, Sengul, Yigit, Serbulent, Kalkan, Goknur, Pancar, Gunseli Sefika, Demir, Helin Deniz, Ates, Omer“…Genomic DNA was isolated and genotyped using PCR assay for the IL-4 gene 70 bp VNTR polymorphism determined by using PCR with the specific primers. RESULTS: There was statistical significance between the groups regarding IL-4 genotype distribution (p<0.001, odds ratio: 2.55 [1.629–4.052], 95% confidence interval) and allele frequencies (p<0.0012.381[1.586–3.617], 95% confidence interval). …”
Publicado 2013
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18892“…We performed a comprehensive analysis of alternative splicing (AS) of REST by rapid amplification of cDNA ends and PCR amplification of cDNAs from various tissues and cell lines with specific primers. We identified 8 novel alternative exons including an alternate last exon which doubles the REST gene boundary, along with numerous 5′/3′ splice sites and ends in the constitutive exons. …”
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18893por Song, Xiaobo, Sun, Jinglu, Mikalsen, Theresa, Roberts, Adam P., Sundsfjord, Arnfinn“…Plasmid replicon typing was performed by multiplex-PCR and sequencing with specific primers for 18 rep-families and 1 unique sequence. …”
Publicado 2013
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18894por Bockelmann, Anna-Christina, Tams, Verena, Ploog, Jana, Schubert, Philipp R., Reusch, Thorsten B. H.“…In this study we quantify the abundance and prevalence of the wasting disease pathogen among 19 Z. marina populations in northern European coastal waters, using quantitative PCR (QPCR) with primers targeting a species specific portion of the internally transcribed spacer (ITS1) of L. zosterae. …”
Publicado 2013
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18895por Lee, Hong Kai, Tang, Julian Wei-Tze, Kong, Debra Han-Lin, Koay, Evelyn Siew-Chuan“…The constant high quality of sequences generated imparts confidence in extending the application of this non-purified amplicon sequencing approach to other gene sequencing assays, with appropriate use of suitably designed primers.…”
Publicado 2013
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18896por Inderbitzin, Patrik, Davis, R. Michael, Bostock, Richard M., Subbarao, Krishna V.“…The DNA sequence alignments are provided and can be used for the design of additional primers.…”
Publicado 2013
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18897por Gmiterek, Anna, Wójtowicz, Halina, Mackiewicz, Paweł, Radwan-Oczko, Małgorzata, Kantorowicz, Małgorzata, Chomyszyn-Gajewska, Maria, Frąszczak, Magdalena, Bielecki, Marcin, Olczak, Mariusz, Olczak, Teresa“…In agreement with these findings, a set of hmuY gene-based primers and standard/real-time PCR with SYBR Green chemistry allowed us to specifically detect P. gingivalis in patients with chronic periodontitis (77.3%) and healthy subjects (20%), the latter possessing lower number of P. gingivalis cells and total bacterial cells. …”
Publicado 2013
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18898“…METHODOLOGY/PRINCIPLE FINDINGS: An array of Th17 related primers for cytokines, chemokines and transcription factors was used in real time reverse transcribed PCR to evaluate gene expression, ELISA for cytokine secretion in the supernatants of antigen stimulated PBMC cultures and flow cytometry for establishing the phenotype of the IL-17, IL-21 producing cells. …”
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18899por Areskog, Marlene, Engström, Annie, Tallkvist, Jonas, von Samson-Himmelstjerna, Georg, Höglund, Johan“…A sequence from C. oncophora (Con-pgp) was identified, showing 83 % similarity to Pgp-9 of Caenorhabditis elegans. Primers specific to putative Con-pgp-9 mRNA were designed, generating a 153-bp PCR product. …”
Publicado 2013
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18900por Fish, Jordan A., Chai, Benli, Wang, Qiong, Sun, Yanni, Brown, C. Titus, Tiedje, James M., Cole, James R.“…To address this, our Functional Gene Pipeline and Repository (FunGene; http://fungene.cme.msu.edu/) offers databases of many common ecofunctional genes and proteins, as well as integrated tools that allow researchers to browse these collections and choose subsets for further analysis, build phylogenetic trees, test primers and probes for coverage, and download aligned sequences. …”
Publicado 2013
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