نتایج جستجو برای: pcr reaction

تعداد نتایج: 548368  

Journal: :Cytokine 1999
L Overbergh D Valckx M Waer C Mathieu

Recently, a novel technique for "real time" quantitative Reverse Transcriptase-PCR which measures PCR-product accumulation during the exponential phase of the PCR reaction using a dual-labelled fluorogenic probe, has been developed. This method allows direct detection of PCR-product formation by measuring the increase in fluorescent emission continuously during the PCR reaction. Here we present...

2011
Qiuying Huang Linlin Zheng Yumei Zhu Jiafeng Zhang Huixin Wen Jianwei Huang Jianjun Niu Xilin Zhao Qingge Li

The target volume of multiplex real-time PCR assays is limited by the number of fluorescent dyes available and the number of fluorescence acquisition channels present in the PCR instrument. We hereby explored a probe labeling strategy that significantly increased the target volume of real-time PCR detection in one reaction. The labeling paradigm, termed "Multicolor Combinatorial Probe Coding" (...

Journal: :Infectious diseases and clinical microbiology 2023

Objective: Reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) is one of the time-saving, accurate, and cost-effective alternative methods to real-time polymerase chain reaction (RT-PCR). This study aimed identify robustness a colorimetric RT-LAMP assay kit that we developed, detecting SARS-COV-2 viral RNA within 30 minutes using primer set special N gene against RT-PCR, gold...

2011
K. Oh A. H. Sklavounos D. J. Marchiarullo N. S. Barker

Utilizing ~1 W of microwave power, we achieved heating of PCR buffer with unprecedented temperature ramp rates that allowed for rapid thermocycling. Polymeric microdevices, chosen for their low cost and ease of fabrication, were constructed from polycarbonate (PC), poly(methyl-methacrylate) (PMMA), and polyester-toner (PeT) using fast, simple microfabrication via computer-aided milling for PC a...

2007
Ali ARSLAN

The origin of horse, dog, cat, bovine, sheep, porcine, and goat meat was determined by the polymerase chain reaction (PCR) technique, using species-specific primers. Test mixtures of meat were prepared by adding 5%, 2.5%, 1%, 0.5%, and 0.1% levels of pork, horse, cat, or dog meat to beef, sheep, and goat meat. Samples taken from those combinations were analyzed by PCR for species determination....

2016
Ian A. Cree

RAS mutation analysis is an important companion diagnostic test. Treatment of colorectal cancer with anti-Epidermal Growth Factor Receptor (EGFR) therapy requires demonstration of RAS mutation status (both KRAS and NRAS), and it is good practice to include BRAF. In Non-Small Cell Lung Cancer (NSCLC) and melanoma, assessment of RAS mutation status can be helpful in triaging patient samples for m...

Journal: :Revista da Sociedade Brasileira de Medicina Tropical 2010
Andrea Cristine Koishi Débora Fonseca Vituri Pedro Sebastião Raimundo Dionízio Filho Alexandre Augusto Sasaki Maria Sueli Soares Felipe Emerson José Venancio

INTRODUCTION Paracoccidioidomycosis is a systemic infection caused by Paracoccidioides brasiliensis. METHODS In this study, a semi-nested PCR for paracoccidioidomycosis diagnosis was developed. The primers ITS1 and ITS4 were used in the first reaction, while the primers MJ03 and ITS1 primer were used in the second reaction. The semi-nested PCR was used to investigate biopsies of five patients...

Journal: :Applied microbiology 2021

With fast-growing polymerase chain reaction (PCR) technologies and various application methods, the technique has benefited science medical fields. While having strengths limitations on each technology, there are not many studies comparing efficiency specificity of PCR technologies. The objective this review is to summarize a large amount scattered information focused two majorly used technolog...

Journal: :Micromachines 2014
Jyh Jian Chen Kun Tze Li Wei Hua Chen Yao-Tsung Yang

This paper illustrates an application of a technique for predicting the thermal characteristics of a bidirectional thermocycling device for polymerase chain reaction (PCR). The micromilling chamber is oscillated by a servo motor and contacted with different isothermal heating blocks to successfully amplify the DNA templates. Because a comprehensive database of contact resistance factors does no...

Journal: :Clinica chimica acta; international journal of clinical chemistry 2015
E Navarro G Serrano-Heras M J Castaño J Solera

Real-time PCR is the method of choice in many laboratories for diagnostic and food applications. This technology merges the polymerase chain reaction chemistry with the use of fluorescent reporter molecules in order to monitor the production of amplification products during each cycle of the PCR reaction. Thus, the combination of excellent sensitivity and specificity, reproducible data, low con...

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