Simplexa Influenza A H1N1 (2009) Kit
Simplexa Influenza A H1N1 (2009) Kit
Background
While the initial threat to world health has been alleviated, H1N1 is different from other flu A viruses and may challenge health care professionals and organizations for years to come. Which is why reliable detection by molecular testing continues to be extremely important especially for higher-risk patient populations.
Why to choose it
Quickly and accurately detect and differentiate H1N1 in your lab.
Benefits
Reliability
100% positive agreement for the H1N1 and influenza A virus.
AGREEMENT WITH COMPOSITE REFERENCE METHOD
2009 H1N1 CLINICAL AGREEMENT
Agreement with composite reference method | Swabs | Aspirates |
Percent Positive Agreement | 100% | 100% |
INFLUENZA A CLINICAL AGREEMENT
Agreement with composite reference method | Swabs | Aspirates |
Percent Positive Agreement | 100% | 100% |
Specimens were determined to be positive for 2009 H1N1 influenza by a composite reference method for the Flu A target including the Luminex xTAG RVP Flu A target, a validated PCR assay using primer and probe sequences published by the CDC and a well characterized PCR followed by sequencing.
Prospectively collected samples. 299 prospectively collected nasal/nasopharyngeal swabs and 112 nasopharyngeal aspirates were analyzed.
For use on
Ordering Info
PRODUCT | CODE | REACTIONS |
Simplexa Influenza A H1N1 Kit | MOL2500 | 100 |
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SIMPLEXA FLU A/B & RSV BROCHURE
- Product: Simplexa Influenza A H1N1 (2009) Kit
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