AltoStar®CMV PCR Kit 1.5 CAN

Specifications Key features Detection and quantification of cytomegalovirus (CMV) specific DNA Health Canada-licensed in vitro diagnostic test Quantification Standards calibrated against the 1 st WHO International Standard for Human Cytomegalovirus for Nucleic Acid Amplification Techniques (NIBSC code: 09/162) Analytical sensitivity reported in IU/ml Limit of Detection (LoD) LoD EDTA plasma 215 IU/ml Sample types The following sample types are validated for use with the AltoStar ® CMV PCR Kit 1.5 CAN: Human EDTA plasma For use with The AltoStar ® CMV PCR Kit 1.5 CAN is configured for use with CFX96™ Deep Well Dx System (Bio-Rad) in combination with the AltoStar ® Automation System AM16, the AltoStar ® Purification Kit 1.5 and the AltoStar ® Internal Control 1.5.