نتایج جستجو برای: nucleic acid amplification

تعداد نتایج: 804699  

Journal: :Biochemical and biophysical research communications 2002
Richard A Collins Lung-Sang Ko King Yip Fung Lok-Ting Lau Jun Xing Albert C H Yu

Nucleic acid sequence-based amplification (NASBA) is an isothermal technique that allows the rapid amplification of specific regions of nucleic acid obtained from a diverse range of sources. It is especially suitable for amplifying RNA sequences. A rapid and specific NASBA technique was developed, allowing the detection of foot-and-mouth disease virus genetic material in a range of sample mater...

Journal: :Journal of clinical microbiology 1999
D S Shapiro

Since it is not possible to state with certainty that contamination has occurred during a nucleic acid amplification assay in the absence of a positive result for a negative control, methods of elementary probability theory are used to illustrate how to identify those runs in which the possibility of contamination should be considered. The use of binomial and Poisson distributions and an analys...

Journal: :Clinical chemistry 2005
Nurith Kurn Pengchin Chen Joe Don Heath Anne Kopf-Sill Kathryn M Stephens Shenglong Wang

BACKGROUND Global analysis of the genome, transcriptome, and proteome is facilitated by the recent development of tools for large-scale, highly parallel analysis. We describe a novel nucleic acid amplification system that generates products by several methods. 3'-Ribo-SPIA primes cDNA synthesis at the 3' polyA tail, and whole transcript (WT)-Ribo-SPIA primes cDNA synthesis across the full lengt...

Journal: :acta medica iranica 0
r. yazdanparast h. sadeghi

cytotoxicity evaluation of daphne mucronata (thymelaeaceae) extract and one of its active purified components, using seven different cancerous cell lines, revealed the strong antiproliferative activity of the plant. using flow cytometry technique, it was found that treatment of the most responsive cells (k562) with the plant extract or the active component inhibited the progression of cells thr...

Journal: :Chemosensors 2021

Several bacteria are known to cause food poisoning; therefore, diagnostic systems that detect essential. Nucleic acid-based testing methods involve polymerase chain reaction (PCR) amplification of great interest due their high sensitivity and specificity. Herein, we developed a syringe-based one-step DNA extraction device streamlines the genomic (gDNA) from within 2 min, enabling versatile appl...

Journal: :Journal of pharmaceutical research international 2021

COVID-19, the infectious pandemic disease is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This deadly was unknown before its catastrophic outbreak of infection in Wuhan city China, December 2019. The situation has increased demand rapid enhancement in-vitro diagnostic assays which would enable mass screening and testing. Several molecular serological diagnostics such ...

Journal: :Molecular and cellular probes 2004
Ales Tichopad Andrea Didier Michael W Pfaffl

Real-time reverse transcription-polymerase chain reaction (RT-PCR) is currently considered the most sensitive method to study low abundance gene expression. Since comparison of gene expression levels in various tissues is often the purpose of an experiment, we studied a tissue-linked effect on nucleic acid amplification. Based on the raw data generated by a LightCycler instrument, we propose a ...

2007
Gustavo Palacios Phenix-Lan Quan Omar J. Jabado Sean Conlan David L. Hirschberg Yang Liu Junhui Zhai Neil Renwick Jeffrey Hui Hedi Hegyi Allen Grolla James E. Strong Jonathan S. Towner Thomas W. Geisbert Peter B. Jahrling Cornelia Büchen-Osmond Heinz Ellerbrok Maria Paz Sanchez-Seco Yves Lussier Pierre Formenty Stuart T. Nichol Heinz Feldmann Thomas Briese W. Ian Lipkin

To facilitate rapid, unbiased, differential diagnosis of infectious diseases, we designed GreeneChipPm, a panmicrobial microarray comprising 29,455 sixty-mer oligonucleotide probes for vertebrate viruses, bacteria, fungi, and parasites. Methods for nucleic acid preparation, random primed PCR amplification, and labeling were optimized to allow the sensitivity required for application with nuclei...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2004
Matthew R Golden James P Hughes Linda E Cles Karen Crouse Katherine Gudgel Jinxin Hu Paul D Swenson Walter E Stamm H Hunter Handsfield

We collected specimens from women who tested positive for Neisseria gonorrhoeae using the Gen-Probe APTIMA Combo 2 (AC2), and we performed confirmatory tests using a nucleic acid amplification test (NAAT) that targets alternate gonococcal nucleic acid sequences. Among 59,664 specimens, 280 (0.47%) had positive results using AC2; 265 of these specimens were tested using the confirmatory NAAT, of...

2012
Hiroko Sudo Atsuko Mizoguchi Junpei Kawauchi Hideo Akiyama Satoko Takizawa

Demand for high quality gene expression data has driven the development of revolutionary microarray technologies. The quality of the data is affected by the performance of the microarray platform as well as how the nucleic acid targets are prepared. The most common method for target nucleic acid preparation includes in vitro transcription amplification of the sample RNA. Although this method re...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید