The paper summarizes the current knowledge of viable PCR, and general recommendations that might be useful for assay optimization are fully discussed.
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A recent study published in the Journal of Clinical Microbiology looked at four commercial chromogenic media for carbapenemase-producing Enterobacteriaceae (CPE)
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The BC-GP test notably expands Nanosphere's infectious disease test capabilities to include fast detection of bacteria that can cause deadly bloodstream infections, an increasingly recognized health threat.
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The kit will be comprised of PathGEN Dx's proprietary reagents, an automated software package, and a contract manufactured GeneChip® microarray from Affymetrix.
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The new BD MAX™ MRSA molecular test has received a Moderate Complexity rating under the Clinical Laboratory Improvement Amendments of 1988 (CLIA '88).
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For diagnostic and public health microbiology, this open access paper examines where whole genome sequencing might be cost effective compared to current alternatives.
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The VACUSIP from INTEGRA provides an ideal benchtop solution for the safe aspiration and disposal of small volumes of liquid waste in clinical, molecular biology, biochemistry and microbiology labs.
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Asynt has announced the availability of new data demonstrating the outstanding performance of its DrySyn Classic heating blocks.
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Public Health Wales is using Luminex's CE marked xTAG Gastrointestinal Pathogen Panel (GPP) for outbreak investigation activities during Olympic and Paralympic training and events taking place in Wales.
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The Quidel Molecular Direct C. difficile Tox A/B assay kit includes an extraction-free, three-step sample preparation process that requires no heat step, no timed step, and no centrifugation as an added benefit.
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With this remarkable system you can test for a comprehensive panel of respiratory pathogens in one, easy-to-use multiplex PCR test that provides results in about an hour.
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The CoolCLAVE™ from AMSBIO is effective in sterilizing and deodorizing lightly contaminated pipettes, pipette tips, gloves, plates, small instruments, and even personal items such as keys and glasses.
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New generation MEDIACLAVE 10/30 systems now provide the feature of digitally signed log files as a safeguard against tampering with downloaded files. Complies with FDA (21CFR Part 11) and EU (GMP Annex 11).
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 | Priorclave Launch Autoclave Performance Analyser
The new system enables Priorclave to provide increased worldwide support ensuring that autoclave users maximise the performance of their steam sterilisers whatever and wherever the application and medium.
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