نتایج جستجو برای: using qrt

تعداد نتایج: 3392536  

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...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Robert L Ferris Liqiang Xi Raja R Seethala Jon Chan Shaun Desai Benjamin Hoch William Gooding Tony E Godfrey

PURPOSE Sentinel node biopsy (SNB) has been shown to accurately stage the regional lymphatics in oral carcinoma. However, intraoperative pathology is only moderately sensitive and final pathology takes several days to complete. The purpose of this study was to develop a rapid, automated, and quantitative real-time PCR (qRT-PCR) assay that can match final pathology in an intraoperative time fram...

ژورنال: :فن آوری زیستی در کشاورزی 0
زهرا طهماسبی استادیار گروه زراعت و اصلاح نباتات، دانشکده کشاورزی، دانشگاه ایلام، ایلام عبدالهادی حسین¬زاده دانشیار گروه زراعت و اصلاح نباتات، پردیس کشاورزی و منابع طبیعی، دانشگاه تهران، کرج هوشنگ علیزاده دانشیار گروه زراعت و اصلاح نباتات، پردیس کشاورزی و منابع طبیعی، دانشگاه تهران، کرج حسن سلطانلو دانشیار گروه زراعت و اصلاح نباتات، دانشکده علوم کشاورزی، دانشگاه کشاورزی و منابع طبیعی گرگان، گرگان

تغذیه گیاهخواران موجب فعال شدن سیستم دفاع مستقیم و غیرمستقیم در گیاه می­شود. به­منظور بررسی نقش تعدادی از ژن­های مؤثر در دفاع مستقیم و یا غیرمستقیم لوبیا در برابر کنه تارتن دولکه­ای، میزان بیان این ژن­ها در تعدادی از ژنوتیپ­های حساس (ژنوتیپ اختر) و مقاوم (ناز و ks41128) لوبیا به کنه دولکه­ای، قبل و بعد از آلودگی به کنه دولکه­ای بوسیله  qrt-pcrمقایسه شد. سپس به­منظور تأیید نتایج آزمایش qrt-pcr، ...

Journal: :genetics in the 3rd millennium 0
الیکا اسماعیل زاده elika esmaeilzadeh مهدی بنان mehdi banan دکترای ژنتیک مولکولی، استادیارمرکز تحقیقات ژنتیک

in this study, several designed creb1-specific shrnas cloned into lentiviral transfer vectors were screened in293t by transient transfection assays. relative creb1 expression was determined by relative qrt-pcr. all of the designed shrnas gave some level of knockdown. one shrna was more effective for knocking down the specific gene among others. the predicted sirnas activities as determined by r...

Journal: :iranian journal of virology 0
f sheikholeslami virology department, pasteur institute of iran, tehran, iran h khanahmadi genetic department, faculty of medical sciences of isfahan university, isfahan, iran m ajorloo virology departments, faculty of medicine, tarbiat modares university, tehran, iran r ahangari cohan pilot nano biotechnology department, pasteur institute of iran, tehran, iran z karimi department of pharmaceutical biotechnology and pharmaceutical sciences research center, school of pharmacy, shiraz university of medical sciences, shiraz, iran d norouzian pilot nano biotechnology department, pasteur institute of iran, tehran, iran

vaccines is considered as a critical point and in-process of quality control (ipqc) test of vaccine production. rapid tests, like real time pcr, are more appropriated when the production occurs at industrial scale because of the amounts of starting materials and the excess of consumed time required. in the current study, a real-time quantitative reverse transcription-polymerase chain reaction (...

Abbas Bahador, Kazem Parivar, Mohammad Hossein Modarressi, Nasim Hayati Rudbari, Niloofar Hassannejad,

Background: Acinetobacter baumannii is an important pathogen in health care and is responsible for severe nosocomial and community-acquired pneumonia. To design novel therapeutic agents, a mouse model for A. baumannii pneumonia is essential. Methods: We described a mouse model of A. baumannii using clinical and 19606R standard strains for developing a quantitative real-time PCR (qRT-PCR) for ra...

2014
Ahmad A Ab-Khader Stefan Krause Ernst Holler

Results Both WT1 antigens induced significant quantities of IFN-g mRNA production after 3 h in the qRT-PCR protocol. Among 18 samples of HLA-A2+, specific responses were detected in 27.8% (5/18) when Db126 peptide, compared to 16.7% (3/18) in the case of WH187 peptide. On the other hand, no detection (0/18) was obtained with ELISPOT, when both WT1 peptides were tested. In four HLA-A2samples nei...

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