نتایج جستجو برای: time quantitative pcr

تعداد نتایج: 2246736  

Journal: :The Annals of occupational hygiene 2011
Jenny Schäfer Peter Kämpfer Udo Jäckel

The thermophilic actinomycete species Saccharopolyspora rectivirgula has been associated with the exogen allergic alveolitis (EAA). EAA is caused by the inhalation of high amounts of airborne spores that can be found for example in environments of agricultural production, compost facilities, mushroom cultivation rooms, or rooms with technical air moistening. Because of the medical relevance of ...

Journal: :Bioinformatics 2017
Stefan Rödiger Michal Burdukiewicz Andrej-Nikolai Spiess Konstantin Blagodatskikh

Motivation Reproducibility, a cornerstone of research, requires defined data formats, which include the setup and output of experiments. The real-time PCR data markup language (RDML) is a recommended standard of the minimum information for publication of quantitative real-time PCR experiments guidelines. Despite the popularity of the RDML format for analysis of quantitative PCR data, handling o...

2012
Abhishek Chaturbedi Liping Yu Mark E Linskey Yi-hong Zhou

1p/19q (1p and/or 19q) deletions are prognostic factors in oligodendroglial tumors (OT) and predict better survival after both chemotherapy and radiotherapy. While studying 1p/19q status as a potential variable within multivariate prognosis models for OT, we have frequently encountered unknown 1p/19q status within our glioma sample database due to lack of paired blood samples for loss of hetero...

Journal: :Biochemical and biophysical research communications 2004
Aleksandar Radonić Stefanie Thulke Ian M Mackay Olfert Landt Wolfgang Siegert Andreas Nitsche

Today, quantitative real-time PCR is the method of choice for rapid and reliable quantification of mRNA transcription. However, for an exact comparison of mRNA transcription in different samples or tissues it is crucial to choose the appropriate reference gene. Recently glyceraldehyde 3-phosphate dehydrogenase and beta-actin have been used for that purpose. However, it has been reported that th...

Journal: :Journal of clinical microbiology 1999
A Pahl U Kühlbrandt K Brune M Röllinghoff A Gessner

Currently, no easy and reliable methods allowing for the quantification of Borrelia burgdorferi in tissues of infected humans or animals are available. Due to the lack of suitable assays to detect B. burgdorferi CFU and the qualitative nature of the currently performed PCR assays, we decided to exploit the recently developed real-time PCR. This technology measures the release of fluorescent oli...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه رازی - دانشکده کشاورزی و منابع طبیعی 1392

بیماری نیوکاسل یکی از مخرب ترین بیماری های ویروسی طیور در سرتاسر جهان است. با توجه به اینکه روش های سنتی قابلیت محدودی در کنترل این بیماری دارند، هدف از انجام این مطالعه استفاده از تکنولوژی های نوین برای تشخیص به موقع بیماری جهت کاهش خسارت پیش روی صنعت طیور می باشد. استخراج rna از واکسن نیوکاسل سویه b1 و با استفاده از کیت rnease mini (شرکت کیاژن، آمریکا) و بر اساس دستورالعمل شرکت سازنده انجام ش...

Journal: :Journal of clinical microbiology 2000
S R Lyons A L Griffen E J Leys

Accurate quantitation of the number of cells of individual bacterial species in dental plaque samples is needed for understanding the bacterial etiology of periodontitis. Real-time PCR offers a sensitive, efficient, and reliable approach to quantitation. Using the TaqMan system we were able to determine both the amount of Porphyromonas gingivalis and the total number of bacterial cells present ...

Journal: :Journal of clinical microbiology 2003
Z Gu S W Belzer C S Gibson M J Bankowski R T Hayden

Adenovirus infection is becoming increasingly recognized as a cause of morbidity and mortality in the immunosuppressed patient population. While early detection and quantitation of adenovirus in peripheral blood has been suggested as a means of directing and monitoring antiviral therapy in these patients, few methods have been published, particularly with respect to viral quantitation. A multip...

Journal: :Journal of clinical microbiology 2000
M H Lin T C Chen T T Kuo C C Tseng C P Tseng

The protozoan Toxoplasma gondii is one of the most common infectious pathogenic parasites and can cause severe medical complications in infants and immunocompromised individuals. We report here the development of a real-time PCR-based assay for the detection of T. gondii. Oligonucleotide primers and a fluorescence-labeled TaqMan probe were designed to amplify the T. gondii B1 gene. After 40 PCR...

Journal: :Journal of clinical microbiology 2000
A Nitsche N Steuer C A Schmidt O Landt H Ellerbrok G Pauli W Siegert

A real-time PCR assay was developed to quantify human cytomegalovirus (CMV) DNA. This assay was used to demonstrate a higher CMV DNA load in plasma of bone marrow transplant patients than in that of blood donors. The CMV load was higher in CMV antigen-positive patients than in antigen-negative patients.

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