نتایج جستجو برای: qrt pcr

تعداد نتایج: 175149  

Journal: :European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 2005
Xiao Tao Wang Wulf Sienel Stephan Eggeling Corina Ludwig Erich Stoelben Johannes Mueller Christoph A Klein Bernward Passlick

OBJECTIVE Detection of disseminated tumor cells in mediastinoscopic biopsies could improve staging and might be helpful concerning indications for neoadjuvant therapy regimens. This prospective study was performed to evaluate a simple and observer-independent polymerase chain reaction (PCR)-based method for the detection of disseminated tumor cells in regional lymph nodes. METHODS Lymph nodes...

Journal: :Antimicrobial agents and chemotherapy 2005
Xiaomin Cai Keith M Woods Steve J Upton Guan Zhu

We report here on a quantitative real-time reverse transcription-PCR (qRT-PCR) assay for assessing drug efficacy against the intracellular pathogen Cryptosporidium parvum. The qRT-PCR assay detects 18S rRNA transcripts from both parasites, that is, the cycle threshold for 18S rRNA from parasites (C(T)([P18S])) and host cells (C(T)([H18S])), and evaluates the relative expression between parasite...

Journal: :Analytical biochemistry 2005
Kent Persson Keith Hamby Luis A Ugozzoli

Quantitative reverse transcription polymerase chain reaction (qRT-PCR) conducted in real time is a powerful tool for measuring messenger RNA (mRNA) levels in biological samples. Multiplex PCR is defined as the simultaneous amplification of two or more DNA (cDNA) targets in a single reaction vessel and may be carried out only using uniquely labeled probes for each target. Up to four genes can be...

2015
Xiaoping Niu Jianmin Qi Gaoyang Zhang Jiantang Xu Aifen Tao Pingping Fang Jianguang Su

To accurately measure gene expression using quantitative reverse transcription PCR (qRT-PCR), reliable reference gene(s) are required for data normalization. Corchorus capsularis, an annual herbaceous fiber crop with predominant biodegradability and renewability, has not been investigated for the stability of reference genes with qRT-PCR. In this study, 11 candidate reference genes were selecte...

2015
Oliver A. Müller Jan Grau Sabine Thieme Heike Prochaska Norman Adlung Anika Sorgatz Ulla Bonas Ya-Wen He

The Gram-negative bacterium Xanthomonas campestris pv. vesicatoria (Xcv) causes bacterial spot disease of pepper and tomato by direct translocation of type III effector proteins into the plant cell cytosol. Once in the plant cell the effectors interfere with host cell processes and manipulate the plant transcriptome. Quantitative RT-PCR (qRT-PCR) is usually the method of choice to analyze trans...

2018
Quanju Xiang Jin Li Peng Qin Maolan He Xiumei Yu Ke Zhao Xiaoping Zhang Menggen Ma Qiang Chen Xiaoqiong Chen Xianfu Zeng Yunfu Gu

Lentinula edodes (shiitake mushroom) is a common edible mushroom with a number of potential therapeutic and nutritional applications. It contains various medically important molecules, such as polysaccharides, terpenoids, sterols, and lipids, were contained in this mushroom. Quantitative real-time polymerase chain reaction (qRT-PCR) is a powerful tool to analyze the mechanisms underlying the bi...

2014
Tamer Z. Salem Walaa R. Allam Suzanne M. Thiem Youjun Zhang

It is challenging to find genes with stable transcripts for use as reference genes for quantitative realtime polymerase chain reaction (qRT-PCR) during viral infection. Autographa californica nucleopolyhedrovirus (AcMNPV) is known to globally shut off host gene transcription in Sf21 cells and to modify their cytoskeletons. In this study, seven host genes were selected for validation as referenc...

2015
Reza Valadan Akbar Hedayatizadeh-Omran Mahdyieh Naghavi Alhosseini-Abyazani Omolbanin Amjadi Alireza Rafiei Mohsen Tehrani Reza Alizadeh-Navaei

Hypoxanthine-guanine phosphoribosyltransferase 1 (HPRT1) is a common housekeeping gene for sample normalization in the quantitative reverse transcriptase polymerase chain (qRT-PCR). However, co-amplification of HPRT1 pseudogenes may affect accurate results obtained in qRT-PCR. We designed a primer pair (HPSF) for pseudogene-free amplification of HPRT1 in qRT-PCR [1]. We showed specific amplific...

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