نتایج جستجو برای: time qpcr

تعداد نتایج: 1899469  

Journal: :European journal of oral sciences 2011
Noel K Childers Robert C Osgood Kuei-Ling Hsu Chanika Manmontri Stephanie S Momeni Harry K Mahtani Gary R Cutter John D Ruby

This study compared SYBR Green real-time quantitative PCR (qPCR) with standard plate counting for the enumeration of Streptococcus mutans in oral samples. Oral samples (n = 710) were collected from high-caries-risk children for quantification of S. mutans by qPCR using primer pairs. The S. mutans copy number was calculated with reference to a qPCR quantification cycle (Cq) standard curve and co...

Journal: :BioTechniques 2008
Heather D VanGuilder Kent E Vrana Willard M Freeman

Following its invention 25 years ago, PCR has been adapted for numerous molecular biology applications. Gene expression analysis by reverse-transcription quantitative PCR (RT-qPCR) has been a key enabling technology of the post-genome era. Since the founding of BioTechniques, this journal has been a resource for the improvements in qPCR technology, experimental design, and data analysis. qPCR a...

Fadyia Mahdi Alameedy, Ghaida Raheem Lateef Al-Awsi, Saade Abdalkareem Jasim, Shireen Ali Obaid,

Background: Epstein-Barr virus (EBV)-associated post-transplant lymphoproliferative disorder (EBV-PTLD) is a known and serious condition for the hematopoietic stem cell transplantation. This study evaluated the prevalence of EBV in umbilical cord samples of healthy pregnant women in Baghdad, Iraq.  Methods: 800 umbilical cord blood (UCB) samples were collected from healthy pregnant women. The ...

Journal: :Methods in molecular biology 2013
Gemma Johnson Tania Nolan Stephen A Bustin

Nucleic acids are the ultimate biomarker and real-time PCR (qPCR) is firmly established as the method of choice for nucleic acid detection. Together, they allow the accurate, sensitive and specific identification of pathogens, and the use of qPCR has become routine in diagnostic laboratories. The reliability of qPCR-based assays relies on a combination of optimal sample selection, assay design ...

Journal: :The American journal of tropical medicine and hygiene 2005
Tasawan Singhsilarak Wattana Leowattana Sornchai Looareesuwan Varee Wongchotigul Ju Jiang Allen L Richards George Watt

Orientia tsutsugamushi infection causes scrub typhus, a common zoonosis of rural Asia. Orientia tsutsugamushi was recently detected by a real-time quantitative polymerase chain reaction (qPCR) assay in animal specimens. We evaluated the same qPCR assay in specimens obtained from patients with serologically proven scrub typhus infections. The 47-kDa qPCR assay was more sensitive than was mouse i...

Journal: :Journal of clinical microbiology 2013
Júlia Gatti Ladeia Costa Ana Carolina Aguiar Vasconcelos Carneiro Alice Thomáz Tavares Gláucia Manzan Queiroz Andrade Daniel Vitor Vasconcelos-Santos José Nélio Januário Daniel Menezes-Souza Ricardo Toshio Fujiwara Ricardo Wagner Almeida Vitor

Real-time PCR (qPCR) was positive in 72/150 (48%) blood samples of newborns with congenital toxoplasmosis. Among infants with active retinochoroiditis, 68% had positive qPCR results, while positivity was 29% (P=0.009) in the absence of ocular involvement. Positive qPCR was associated with the presence of retinochoroidal lesions, with an odds ratio of 2.8.

2016
Narciso M. Quijada Gislaine Fongaro Célia R. M. Barardi Marta Hernández David Rodríguez-Lázaro

The increase of foodborne viral outbreaks highlights the need for a rapid and sensitive method for the prediction of viral infectivity in food samples. This study assesses the use of propidium monoazide (PMA) coupled with real-time PCR methods (RT-qPCR or qPCR for RNA or DNA viruses, respectively) in the determination of viral infectivity in complex animal-related food matrices. Clam and Spanis...

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