نتایج جستجو برای: quantification pcr

تعداد نتایج: 251724  

Journal: :The International journal of developmental biology 2006
Erik Willems Ileana Mateizel Caroline Kemp Greet Cauffman Karen Sermon Luc Leyns

Embryonic Stem (ES) cells have the potential to form every cell of the body and thus are of great promise for tissue transplantation. One of the rising techniques that allows studying the differentiation state of ES cells is quantitative RT-PCR (qRT-PCR). When relative quantification by qRT-PCR is applied, accurate normalization is necessary, since differentiated embryonic stem cells and develo...

Journal: :Journal of clinical microbiology 2011
Hui Nie Alison A Evans W Thomas London Timothy M Block Xiangdong David Ren

Hepatitis B virus (HBV) carrying the A1762T/G1764A double mutation in the basal core promoter (BCP) region is associated with HBe antigen seroconversion and increased risk of liver cirrhosis and hepatocellular carcinoma (HCC). Quantification of the mutant viruses may help in predicting the risk of HCC. However, the viral genome tends to have nucleotide polymorphism, which makes it difficult to ...

Journal: :Journal of clinical microbiology 2001
T C Harder M Hufnagel K Zahn K Beutel H J Schmitt U Ullmann P Rautenberg

Detection of parvovirus B19 DNA offers diagnostic advantages over serology, particularly in persistent infections of immunocompromised patients. A rapid, novel method of B19 DNA detection and quantification is introduced. This method, a quantitative PCR assay, is based on real-time glass capillary thermocycling (LightCycler [LC]) and fluorescence resonance energy transfer (FRET). The PCR assay ...

2015
Hannah Yu Yoonsoo Hahn Inchul Yang Osman El-Maarri

Most contemporary methods for the quantification of DNA methylation employ bisulfite conversion and PCR amplification. However, many reports have indicated that bisulfite-mediated PCR methodologies can result in inaccurate measurements of DNA methylation owing to amplification biases. To calibrate analytical biases in quantification of gene methylation, especially those that arise during PCR, w...

Journal: :Clinical chemistry 1995
B Debuire O Sol A Lemoine E May

We report an original application of competitive reverse transcription-polymerase chain reaction (RT-PCR) for the quantification of MDR1 mRNA in clinical specimens by simultaneous reverse transcription and PCR amplification of cellular RNA with decreasing amounts of an internal standard. The competitor RNA shares the same MDR1 primer sequences as the cellular mRNA, but yields a different-sized ...

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