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The new method described here may be useful for simultaneous detection and subtyping of major influenza A viruses.
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A multiplex reverse-transcriptase polymerase chain reaction (mRT-PCR) assay was designed for simultaneous detection and differentiation of avian H3, H5, H9 subtype AIVs and NDVs.
In summary, we have developed a dual-functional system for simultaneous detection and removal of formaldehyde.
Spoligotyping, a new method for simultaneous detection and typing of M. tuberculosis complex bacteria, has been recently developed (9– 11).
This report describes a re-sequencing pathogen microarray (RPM -based assay foRPM -basedeous detection, identificassay and characterization oforny simultaneousype A human or avian influenza virus, basedetectiond, sensidentificationimen-specific determinandon of nucharacterizationes frof viranyhemagglutinin, neuraminidasubtype ofher genes.
We consider the presented assays to be well suited for the detection and subtyping of circulating influenza viruses.
There are many molecular techniques for detection and subtyping of IAVs.
In this paper we present a technique aimed for simultaneous detection of multiple types of gold nanoparticles (GNPs) within a biological sample, using lock-in detection.
These SWNT forest arrays can be used to interfacing with microfluidic for simultaneous detection of different types of proteins [89].
The device is suitable for simultaneous detection of multiple types of biomolecules.
While this massively parallel technique allows for simultaneous detection of hundreds to hundreds of thousands of SNPs [16], [17], it requires a priori knowledge of the relevant polymorphisms.
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