By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – Luminex said after the close of the market on Tuesday that the US Food and Drug Administration has given 510(k) clearance for its xTag Respiratory Viral Panel Fast.

The panel includes respiratory syncytial virus; influenza A; non-specific influenza A; H1 subtype; H3 subtype; influenza B; metapneumovirus; adenovirus; and entero-rhinovirus.

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A research duo estimates in PLOS One the number of papers that have used misidentified cell lines.

UK's National Institute for Health and Care Excellence approves GlaxoSmithKline's SCID gene therapy despite cost.

Science reports that Brazilian researchers are petitioning for the reversal of budget cuts.

In PLOS this week: gene flow patterns in common ash, guidelines for using morpholinos in zebrafish, and more.