RealStar® CCHFV RT-PCR Kit

  • Detection of Crimean Congo Haemorrhagic Fever Virus (CCHFV) specific RNA
  • Parallel Testing within Tropical RT-PCR Test Kit Panel
  • Ready-to-use Kit including Internal and Positive Control
  • CE IVD marked in vitro diagnostic test
Dilution series of CCHFV specific RNA, ranging from 101 to 104 copies/µl, detected in the FAM detection channel [A]. The
Internal Control (IC) is detected in the JOE detection channel [B].
Prod. No Product For use with
181013 RealStar® CCHFV RT-PCR Kit 1.0
Download Manual (PDF)
Version 01/2017
Mx 3005P™ QPCR System, VERSANT® kPCR Molecular System AD, ABI Prism® 7500 SDS and 7500 Fast SDS, LightCycler® 480 Instrument II, Rotor-Gene® 6000, Rotor-Gene® Q 5/6 plex Platform, CFX96™ Real-Time System

 

Please find here further important information or other useful references:

 

Material Safety Data Sheet (PDF) 

Declaration of conformity (PDF)

 

 

Product not licensed with Health Canada and not FDA cleared or approved.

altona Diagnostics GmbH
Mörkenstr. 12
22767 Hamburg
Germany

phone +49 40 548 06 76 - 0
fax +49 40 548 06 76 - 10
e-mail info@altona-diagnostics.com