نتایج جستجو برای: pcr amplification

تعداد نتایج: 218216  

Journal: :Clinical chemistry 1999
C C Raggi M L Bagnoni G P Tonini M Maggi G Vona P Pinzani K Mazzocco B De Bernardi M Pazzagli C Orlando

BACKGROUND Neuroblastoma is the most common extracranial malignant solid tumor in children under 5 years and is characterized by a wide clinical and biological heterogeneity, from spontaneously regressive forms to cancers with a rapid and fatal progression. MYCN oncogene amplification is considered the most important prognostic factor to evaluate survival and therapeutic choices in these patien...

Journal: :Lab on a chip 2010
Maximilian Focke Fabian Stumpf Günter Roth Roland Zengerle Felix von Stetten

Pre-amplification is a basis for numerous polymerase chain reaction (PCR) protocols but bears severe contamination risks due to handling of high-copy DNA samples. Therefore we developed a self-contained centrifugal microfluidic system comprising pre-stored reagents; it enables pre-amplification of specific DNA sequences prior to automated aliquoting and real-time PCR in a modified commercial th...

Journal: :Clinical chemistry 1997
N J Gibson H L Gillard D Whitcombe R M Ferrie C R Newton S Little

We combined the amplification refractory mutation system (ARMS) and fluorescence polarization (FP) to give a homogeneous genomic DNA genotype analysis method. Oligonucleotide probes labeled with the fluorescein dyes fluorescein isothiocyanate and 5-([4,6-dichlorotriazin-2-yl]amino)fluorescein and the rhodamine dye 6-carboxyrhodamine were included in amplification mixes and were annealed to PCR ...

Journal: :CoRR 2004
Kishori M. Konwar Ion I. Mandoiu Alexander Russell Alexander A. Shvartsman

A critical problem in the emerging high-throughput genotyping protocols is to minimize the number of polymerase chain reaction (PCR) primers required to amplify the single nucleotide polymorphism loci of interest. In this paper we study PCR primer set selection with amplification length and uniqueness constraints from both theoretical and practical perspectives. We give a greedy algorithm that ...

Journal: :medical journal of islamic republic of iran 0
m nasrollahei from the dept. of microbiology, sari medical school, khazar boulevard, sari, i.r. iran. hg robson

we investigated the use of dna amplification by polymerase chain reaction (per) for detection of mycobacterium tuberculosis in 300 patients who were suspected of having pulmonary tuberculosis and compared the results with culture results which were performed in parallel with pcr. two-thirds of each sample was processed for smear and culture by standard methods and one-third was prepared for dna...

A. Jamshidi S. Afshari-Nic T. Zahraei-Salehi

  A total of 60 neck skin swab samples were taken from 12 different broiler flocks after the chilling stage of processing at a commercial broiler slughtering facility in Mashhad. The presence of Salmonella was assessed by conventional culture method and confirmed by using poly O and poly H antiserum in serotyping. PCR amplification of invA gene as a specific method for detection of Salmonella w...

Berigiteh Eckert Elaheh Ebrahimzadeh Nastaran Sadr Shirazi, Parviz Shayan Sedigheh Jafari

BACKGROUND: A major issue in many gene expressionstudies utilizing small amount of biological materials is thelimited quantity of RNApurified from clinical samples, which isoften used for RT-PCR or standard Northern blot analysis.OBJECTIVES: The SMART cDNA synthesis method and subsequentSMART-cDNA-PCR technique was used to analyse 3genes in macroschizonts of Theileria annulata in small lymphnod...

Journal: :journal of arthropod-borne diseases 0
f karimian department of medical entomology and vector control, school of public health, tehran university of medical sciences, tehran, iran mm sedaghat department of medical entomology and vector control, school of public health, tehran university of medical sciences, tehran, iran ma oshaghi department of medical entomology and vector control, school of public health, tehran university of medical sciences, tehran, iran f mohtarami department of medical entomology and vector control, school of public health, tehran university of medical sciences, tehran, iran a sanei dehkordi department of medical entomology and vector control, school of public health, tehran university of medical sciences, tehran, iran m koosha department of medical entomology and vector control, school of public health, tehran university of medical sciences, tehran, iran

background : appropriate methodology for storage biological materials, extraction of dna, and proper dna preservation is vital for studies involving genetic analysis of insects, bacteria, and reservoir hosts as well as for molecular diagnostics of pathogens carried by vectors and reservoirs. here we tried to evaluate the utility of a simple filter paper-based for storage of insects, bacteria, r...

2014
Naoki Tanigawa Toshitsugu Fujita Hodaka Fujii

Polymerase chain reaction (PCR) amplification of multiple templates using common primers is used in a wide variety of molecular biological techniques. However, abundant templates sometimes obscure the amplification of minor species containing the same primer sequences. To overcome this challenge, we used oligoribonucleotides (ORNs) to inhibit amplification of undesired template sequences withou...

2014
Zhiyuan Wu Yunqing Zhang Xinju Zhang Xiao Xu Zhihua Kang Shibao Li Chen Zhang Bing Su Ming Guan

A multiplex snapback primer system was developed for the simultaneous detection of JAK2 V617F and MPL W515L/K mutations in Philadelphia chromosome- (Ph-) negative myeloproliferative neoplasms (MPNs). The multiplex system comprises two snapback versus limiting primer sets for JAK2 and MPL mutation enrichment and detection, respectively. Linear-After exponential (LATE) PCR strategy was employed f...

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