Background: Genome walking is a DNA-cloning methodology that is used to isolate unknown genomic regions adjacent to known sequences. However, the existing genome-walking methods have their own limitations. Objectives: Our aim was to provide a simple and efficient genome-walking technology. Material and Methods: In this paper, we dev...

Molecular detection techniques are believed to be key tools for both prevention and treatment follow up of brucellosis within live stock and human beings. Consequently rapid, reliable, easy to perform and automated systems for Brucella detection are urgently needed to allow early diagnosis and adequate antibiotic therapy in time. Brucellosis is a worldwide re-emerging zoonosis causing high econ...

The Tenuivirus maize stripe virus (MStV) shares many properties with viruses in the genus Phlebovirus of the family Bunyaviridae. Besides genome organization and gene expression strategies, one property shared by these plant- and vertebrate-infecting viruses is that transcription gives rise to virus-specific mRNAs containing nonviral 5'-terminal nucleotide sequences. The 5'-terminal nucleotides...

conclusions the results of the present study showed that in comparison with previously published primer sets, p. aeruginosa infection can be diagnosed with higher sensitivity and specificity by the conventional pcr assay using the newly designed primers. it was also shown that the results of the pcr assay on clinical samples of severe infections became positive much earlier than the results of ...

Multiplex PCR can be used to simultaneously screen for pathogenic and nonpathogenic strains of E. coli using strain-specific primer pairs. By using at least two strain-specific primer pairs for each organism, and replicate sample reactions, it is possible to reliably detect the presence of >10 genome equivalents. In this example, two food samples were analyzed for the presence of a specific pat...

In order to provide feasible primer sets for performing a polymerase chain reaction (PCR) experiment, many primer design methods have been proposed. However, the majority of these methods require a long time to obtain an optimal solution since large quantities of template DNA need to be analyzed, and the designed primer sets usually do not provide a specific PCR product size. In recent years, p...