نتایج جستجو برای: qpcr

تعداد نتایج: 13261  

2017
Samuel Dorevitch Abhilasha Shrestha Stephanie DeFlorio-Barker Cathy Breitenbach Ira Heimler

BACKGROUND The United States Environmental Protection Agency has established methods for testing beach water using the rapid quantitative polymerase chain reaction (qPCR) method, as well as "beach action values" so that the results of such testing can be used to make same-day beach management decisions. Despite its numerous advantages over culture-based monitoring approaches, qPCR monitoring ha...

Journal: :Applied and environmental microbiology 2010
Christoph Tellenbach Christoph R Grünig Thomas N Sieber

A nested single-copy locus-based quantitative PCR (qPCR) assay and a multicopy locus-based qPCR assay were developed to estimate endophytic biomass of fungal root symbionts belonging to the Phialocephala fortinii sensu lato-Acephala applanata species complex (PAC). Both assays were suitable for estimation of endophytic biomass, but the nested assay was more sensitive and specific for PAC. For m...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پایه 1392

فرآیند ترمیم در سیستم عصبی، پیچیده بوده و چالشی بزرگ برای محققان می باشد. رویکرد مهندسی بافت با استفاده از ترکیب سلول های بنیادی و داربست های نانوفیبری علاقه ی جامعه ی تحقیق را برای کاربردهای بازسازی بافت عصبی به خود جلب کرده است. هدف از تحقیق حاضر، مطالعه ی پتانسیل تمایزی سلول های بنیادی پرتوان القایی انسانی (hipscs) به دودمان های عصبی بر روی داربست های پلی اترسولفون (pes)، pes پلاسما شده و pe...

Journal: :Current issues in molecular biology 2010
J M Gallup F B Sow A Van Geelen M R Ackermann

Real-time quantitative polymerase chain reaction is subject to inhibition by substances that co-purify with nucleic acids during isolation and preparation of samples. Such materials alter the activity of reverse transcriptase (RT) and thermostable DNA polymerase enzymes on which the assay depends. When removal of inhibitory substances by column or reagent-based methods fails or is incomplete, t...

2017
Sergio Araujo Luiz Ricardo Goulart Richard W Truman Isabela Maria B Goulart Varalakshmi Vissa Wei Li Masanori Matsuoka Philip Suffys Amanda B Fontes Patricia S Rosa David M Scollard Diana L Williams

BACKGROUND Real-Time PCR-High Resolution Melting (qPCR-HRM) analysis has been recently described for rapid drug susceptibility testing (DST) of Mycobacterium leprae. The purpose of the current study was to further evaluate the validity, reliability, and accuracy of this assay for M. leprae DST in clinical specimens. METHODOLOGY/PRINCIPAL FINDINGS The specificity and sensitivity for determinin...

2015
Zhanguo Chen Yongqing Tong Yan Li Qingping Gao Qiongyu Wang Chaohong Fu Zunen Xia

Rapid diagnosis of acute promyelocytic leukemia (APL) with promyelocytic leukemia-retinoic acid receptor alpha (PML-RARa) contributes to a highly effective therapy with all-trans retinoic acid (ATRA). Real-time quantitative reverse transcription-polymerase chain reaction (RT-qPCR) is a valuable tool to diagnose APL with PML-RARa. However, a single RT-qPCR analysis, which is laborious and costly...

Journal: :Experimental parasitology 2013
Rongchang Yang Cain Murphy Yong Song Josephine Ng-Hublin Annika Estcourt Nawal Hijjawi Rachel Chalmers Stephen Hadfield Andrew Bath Cameron Gordon Una Ryan

Cryptosporidium is an enteric protozoan parasite that is resistant to inactivation by commonly used drinking water disinfectants. Between 2004 and 2010, it was responsible for 60% of all waterborne protozoan parasitic outbreaks reported worldwide. Most sporadic infections in humans and almost all outbreaks are caused by Cryptosporidium parvum and Cryptosporidium hominis. We report the developme...

2014
Fernanda Gutierrez-Rodrigues Bárbara A. Santana-Lemos Priscila S. Scheucher Raquel M. Alves-Paiva Rodrigo T. Calado

Telomere length measurement is an essential test for the diagnosis of telomeropathies, which are caused by excessive telomere erosion. Commonly used methods are terminal restriction fragment (TRF) analysis by Southern blot, fluorescence in situ hybridization coupled with flow cytometry (flow-FISH), and quantitative PCR (qPCR). Although these methods have been used in the clinic, they have not b...

Journal: :BMC Infectious Diseases 2008
Prasanna D Khot Daisy L Ko Robert C Hackman David N Fredricks

BACKGROUND The diagnosis of invasive pulmonary aspergillosis (IPA) remains challenging. Culture and histopathological examination of bronchoalveolar lavage (BAL) fluid are useful but have suboptimal sensitivity and in the case of culture may require several days for fungal growth to be evident. Detection of Aspergillus DNA in BAL fluid by quantitative PCR (qPCR) offers the potential for earlier...

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