- Zunehmende Verbreitung des therascreen® KRAS RGQ PCR Kits und des Rotor-Gene Q MDx Instruments
- Clarient-Netzwerk mit über 2.000 Pathologen setzt auf das therascreen KRAS RGQ PCR Kit, das einzige FDA-zugelassene KRAS-Begleitdiagnostikum für Erbitux® zur Behandlung von Patienten mit metastasierendem Darmkrebs
- KRAS-Test ebnet den Weg für die Einführung weiterer Produkte aus QIAGENs wachsender Pipeline für die personalisierte Medizin
QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) hat heute bekanntgegeben, dass Clarient - ein Tochterunternehmen der GE Healthcare Company und ein führendes US-Servicelabor in der Krebsdiagnostik - das therascreen® KRAS RGQ PCR Kit (therascreen KRAS-Test) ab sofort
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