نتایج جستجو برای: taqman probe

تعداد نتایج: 97576  

Journal: :Journal of agricultural and food chemistry 2008
Sergio Salvi Fabio D'Orso Giorgio Morelli

Many countries have introduced mandatory labeling requirements on foods derived from genetically modified organisms (GMOs). Real-time quantitative polymerase chain reaction (PCR) based upon the TaqMan probe chemistry has become the method mostly used to support these regulations; moreover, event-specific PCR is the preferred method in GMO detection because of its high specificity based on the f...

2017

In order to minimize the adverse environmental impact of packaging and shipping products on dry ice, Life Technologies investigated the feasibility of shipping its TaqMan® Assay products at ambient temperature. This report describes stability and performance testing of three classes of assays (TaqMan® Gene Expression Assays, TaqMan® MicroRNA Assays, and TaqMan® SNP Genotyping Assays) after subj...

Journal: :Journal of clinical microbiology 2006
Hasan Yesilkaya Francesca Meacci Stefan Niemann Doris Hillemann Sabine Rüsch-Gerdes Michael R Barer Peter W Andrew Marco R Oggioni

The ability of fluorescence resonance energy transfer, molecular-beacon, and TaqMan probes to detect single nucleotide polymorphism (SNP) in the presence of a wild-type allele was evaluated using drug resistance-conferring SNPs in mixed Mycobacterium tuberculosis DNA. It was found that both the absolute quantity and the ratio of alleles determine the detection sensitivity of the probe systems.

2012
Weiyi Ni Caroline Le Guiner Philippe Moullier Richard O. Snyder

Sensitive and specific tests for detecting exogenous DNA molecules are useful for infectious disease diagnosis, gene therapy clinical trial safety, and gene doping surveillance. Taqman real-time PCR using specific sequence probes provides an effective approach to accurately and quantitatively detect exogenous DNA. However, one of the major challenges in these analyses is to eliminate false posi...

2013
C.A.G. Leal G.A. Carvalho-Castro A.C. Cottorello R.C. Leite H.C.P. Figueiredo

The aims of this study were to standard and optimize a qPCR protocol with FAM-BHQ1 probe, and to compare its sensitivity against TaqMan qPCR and PCR methods to diagnose shrimp WSD. The FAM-BHQ1 qPCR presented higher clinical sensitivity and showed to be a robust alternative to detect WSSV in clinical samples.

2009
Nozomu Hanaoka Minenosuke Matsutani Hiroki Kawabata Seigo Yamamoto Hiromi Fujita Akiko Sakata Yoshinao Azuma Motohiko Ogawa Ai Takano Haruo Watanabe Toshio Kishimoto Mutsunori Shirai Ichiro Kurane Shuji Ando

We developed a specific and rapid detection system for Rickettsia japonica and R. heilongjiangensis, the causative agents of spotted fever, using a TaqMan minor groove binder probe for a particular open reading frame (ORF) identified by the R. japonica genome project. The target ORF was present only in R. japonica-related strains.

Journal: :hepatitis monthly 0
bahman khalvati fahlyani diagnosis laboratory sciences and technology research center, school of paramedical, sciences shiraz university of medical sciences, shiraz, ir iran abbas behzad-behbahani diagnosis laboratory sciences and technology research center, school of paramedical, sciences shiraz university of medical sciences, shiraz, ir iran; department of biotechnology, school of paramedical sciences, shiraz university of medical sciences, shiraz, ir iran; diagnosis laboratory sciences and technology research center, school of paramedical, sciences shiraz university of medical sciences, shiraz, ir iran. tel: +98-7132270301, fax: +98-7132270301 seiied alireza taghavi gastroenterohepatology research center, shiraz university of medical sciences, shiraz, ir iran ali farhadi diagnosis laboratory sciences and technology research center, school of paramedical, sciences shiraz university of medical sciences, shiraz, ir iran; department of biotechnology, school of paramedical sciences, shiraz university of medical sciences, shiraz, ir iran saeede salehi diagnosis laboratory sciences and technology research center, school of paramedical, sciences shiraz university of medical sciences, shiraz, ir iran; department of biotechnology, school of paramedical sciences, shiraz university of medical sciences, shiraz, ir iran setare adibzadeh diagnosis laboratory sciences and technology research center, school of paramedical, sciences shiraz university of medical sciences, shiraz, ir iran; department of biotechnology, school of paramedical sciences, shiraz university of medical sciences, shiraz, ir iran

conclusions the quite sensitive in-house taqman real time rt-pcr assay was able to detect and quantify all four main hcv genotypes prevailing around all geographical regions of iran. results the lower limit detection of this in-house hcv real-time rt-pcr was determined as 100 rna copies/ml. inter- and intra-assay coefficient of variation (cv) of this in-house hcv real-time rt-pcr ranged from 0....

2012
Dawn N. Birdsell Talima Pearson Erin P. Price Heidie M. Hornstra Roxanne D. Nera Nathan Stone Jeffrey Gruendike Emily L. Kaufman Amanda H. Pettus Audriana N. Hurbon Jordan L. Buchhagen N. Jane Harms Gvantsa Chanturia Miklos Gyuranecz David M. Wagner Paul S. Keim

Single nucleotide polymorphisms (SNPs) are abundant in genomes of all species and biologically informative markers extensively used across broad scientific disciplines. Newly identified SNP markers are publicly available at an ever-increasing rate due to advancements in sequencing technologies. Efficient, cost-effective SNP genotyping methods to screen sample populations are in great demand in ...

Journal: :FEMS immunology and medical microbiology 2000
M Guiver R Borrow J Marsh S J Gray E B Kaczmarski D Howells P Boseley A J Fox

In a period where the proportion of culture confirmed cases in the UK has been steadily declining, diagnosis by PCR has been used to increase the number of confirmed cases and provide additional epidemiological data. This report presents a comparative evaluation of the fluorogenic probe-based 5' exonuclease assay (Taqman) using the Perkin-Elmer Applied Biosystems automated sequence detection sy...

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