نتایج جستجو برای: pcr based marker

تعداد نتایج: 3177678  

Journal: :The Southeast Asian journal of tropical medicine and public health 2009
Pheravut Wongsawad Chalobol Wongsawad

Haplorchis taichui specific primers were designed using a high annealing temperature random amplified polymorphic DNA (HAT-RAPD) PCR method and 18 arbitrary primers (Operon Technologies) to generate polymorphic DNA profiles for 13 different parasites. The H. taichui specific fragment was screened. A 256 bp HAT-RAPD marker generated from OPP-11 primer specific for H. taichui was cloned and seque...

2012
John M Gaspar W Kelley Thomas

Background Early marker-based metagenomic studies, such as those of the human microbiome, were performed without properly accounting for the effects of noise (pyrosequencing errors, PCR single-base errors, and PCR chimeras). One popular solution to address these issues is to utilize AmpliconNoise [1]. This collection of algorithms was validated on mock community datasets in which the ‘correct’ ...

2007
ATA-UR-REHMAN BEN STODART

A simple and reliable method for extracting genomic DNA from leaf and seed of monocotyledonous and dicotyledonous plants and ascomycete fungal mycelium is described. The method requires only 50mg of sample and yields approximately 10μg of high quality DNA. It involves inexpensive, non-organic constituents and can reliably be used for the parallel isolation of 384 DNA samples suitable for PCR ba...

TrnL-F region including intron trnL (UAA) and trnL (UAA) - trn (GAA) spacer in the large single-copy region of the chloroplast genome is widely used to infer phylogenetic relationships in plants. In this study, we obtained the trnL-F sequences from 8 samples of Arum L. in Iran. Phylogenetic analyses were conducted by the Bayesian inference, maximum parsimony, and maximum likelihood methods. The...

Journal: :Acta biochimica Polonica 2004
Anna Fabisiewicz Jadwiga Kulik Paulina Kober Elzbieta Brewczyńska Tadeusz Pieńkowski Janusz A Siedlecki

The aim of this study was to use a two-marker assay for the detection of breast cancer cells circulating in patients' blood. We have applied a PCR-based methodology to follow up the possibility of the development of metastatic disease in stage I and II patients who had undergone curative surgery. Since the number of circulating cancer cells in peripheral blood is very low, the technique for the...

Journal: :Journal of environmental management 2014
Timothy E Riedel Amity G Zimmer-Faust Vanessa Thulsiraj Tania Madi Kaitlyn T Hanley Darcy L Ebentier Muruleedhara Byappanahalli Blythe Layton Meredith Raith Alexandria B Boehm John F Griffith Patricia A Holden Orin C Shanks Stephen B Weisberg Jennifer A Jay

Some molecular methods for tracking fecal pollution in environmental waters have both PCR and quantitative PCR (qPCR) assays available for use. To assist managers in deciding whether to implement newer qPCR techniques in routine monitoring programs, we compared detection limits (LODs) and costs of PCR and qPCR assays with identical targets that are relevant to beach water quality assessment. Fo...

Journal: :Yeast 1995
D C Amberg D Botstein E M Beasley

We adapted a fusion polymerase chain reaction (PCR) strategy to synthesize gene disruption alleles of any sequenced yeast gene of interest. The first step of the construction is to amplify sequences flanking the reading frame we want to disrupt and to amplify the selectable marker sequence. Then we fuse the upstream fragment to the marker sequence by fusion PCR, isolate this product and fuse it...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه یزد - دانشکده زبانهای خارجی 1392

abstract since heubners (1985) pioneering study, there have been many studies on (mis) use/ non-use of articles by l2 learners from article-less and article languages. the present study investigated how persian l2 learners of english produce and interpret english definite descriptions and demonstrative descriptions. it was assumed that definite and demonstrative descriptions share the same cen...

2014
Maria W. Smith Andrei L. Ghindilis Ihab A. Seoudi Kenneth Smith Rosalind Billharz Holly M. Simon

PCR multiplexing has proven to be challenging, and thus has provided limited means for pathogen genotyping. We developed a new approach for analysis of PCR amplicons based on restriction endonuclease digestion. The first stage of the restriction enzyme assay is hybridization of a target DNA to immobilized complementary oligonucleotide probes that carry a molecular marker, horseradish peroxidase...

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