نتایج جستجو برای: qrt pcr

تعداد نتایج: 175149  

Journal: :Croatian medical journal 2005
Davorka Sutlović Marija Definis Gojanović Simun Andelinović Dijana Gugić Dragan Primorac

AIM To investigate the dose-response effect of humic acid (HA) on the quantitative real time polymerase chain reaction (QRT-PCR) inhibition and the efficiency of Taq polymerase increment in preventing inhibition by HA in DNA extracted from ancient bones. METHODS DNA was isolated from bone samples and DNA quantification was conducted with the real-time 5' exonuclease detection assay (TaqMan), ...

2012
Natalia V. Demidenko Aleksey A. Penin

qRT-PCR is a generally acknowledged method for gene expression analysis due to its precision and reproducibility. However, it is well known that the accuracy of qRT-PCR data varies greatly depending on the experimental design and data analysis. Recently, a set of guidelines has been proposed that aims to improve the reliability of qRT-PCR. However, there are additional factors that have not bee...

2015
Wei-Lin Fu Sheng-Ren Sun Hua-Ying Fu Ru-Kai Chen Jin-Wei Su San-Ji Gao

Sugarcane mosaic disease is caused by the Sugarcane streak mosaic virus (SCSMV; genus Poacevirus, family Potyviridae) which is common in some Asian countries. Here, we established a protocol of a one-step real-time quantitative reverse transcription PCR (real-time qRT-PCR) using the TaqMan probe for the detection of SCSMV in sugarcane. Primers and probes were designed within the conserved regio...

2011
Vera Lúcia Teixeira de Freitas Sheila Cristina Vicente da Silva Ana Marli Sartori Rita Cristina Bezerra Elizabeth Visone Nunes Westphalen Tatiane Decaris Molina Antonio R. L. Teixeira Karim Yaqub Ibrahim Maria Aparecida Shikanai-Yasuda

BACKGROUND Reactivation of chronic Chagas disease, which occurs in approximately 20% of patients coinfected with HIV/Trypanosoma cruzi (T. cruzi), is commonly characterized by severe meningoencephalitis and myocarditis. The use of quantitative molecular tests to monitor Chagas disease reactivation was analyzed. METHODOLOGY Polymerase chain reaction (PCR) of kDNA sequences, competitive (C-) PC...

Journal: :Journal of clinical microbiology 2015
Timothy R Southern Lori D Racsa César G Albariño Paul D Fey Steven H Hinrichs Caitlin N Murphy Vicki L Herrera Anthony R Sambol Charles E Hill Emily L Ryan Colleen S Kraft Shelley Campbell Tara K Sealy Amy Schuh James C Ritchie G Marshall Lyon Aneesh K Mehta Jay B Varkey Bruce S Ribner Kent P Brantly Ute Ströher Peter C Iwen Eileen M Burd

Rapid, reliable, and easy-to-use diagnostic assays for detection of Zaire ebolavirus (ZEBOV) are urgently needed. The goal of this study was to examine the agreement among emergency use authorization (EUA) tests for the detection of ZEBOV nucleic acids, including the BioFire FilmArray BioThreat (BT) panel, the FilmArray BT-E panel, and the NP2 and VP40 quantitative real-time reverse transcripta...

Journal: :Daehan binyogi jong-yang haksulji 2022

Purpose: The aims of this study were to investigate the clinical value Rab27a as a urinary biomarker, and its efficiency in prediction bladder cancer grade.Materials Methods: expression urine samples patients with cancer, cell line (T-24), tissue was estimated via quantitative reverse transcription polymerase chain reaction (qRT-PCR). level investigated according sex, age, histological grade qR...

Journal: :Methods in molecular biology 2010
Gary J Latham

Proper normalization of quantitative RT-PCR (qRT-PCR) data is a crucial component of gene -expression analysis. Although arbitrarily selected housekeeping genes have been used to normalize many published mRNA RT-PCR datasets, there is a growing awareness that such normalizers should be first validated empirically. The use of stable reference genes is particularly needed for qRT-PCR of microRNA ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید