Simplexa Bordetella Universal Direct Kit
Simplexa Bordetella Universal Direct Kit
Background
The World Health Organization estimates that there are 50 million whooping cough cases worldwide each year, resulting in 350,000 deaths. Pertussis, caused by Bordetella pertussis, can be detected among all age groups (e.g., neonates, children, adolescents and adults). While a great majority of these cases are caused by B. pertussis, up to 20% of cases are caused by Bordetella parapertussis, which can present clinically as a milder pertussis-like disease.
Why to choose it
A high-throughput, simplified workflow with broad coverage, including both B. pertussis and B. parapertussis, without DNA extraction that provides results in about an hour.
For use on
Benefits
Simple and Dependable Bordetella Testing
The Simplexa Bordetella Universal Direct assay provides results in about an hour direct from nasopharyngeal swabs without the need for DNA isolation.
Reliability
Reliable performance that you can count on
The Simplexa Bordetella Universal Direct assay has 98.5% and 100% sensitivity for B. pertussis and B. parapertussis respectively.
SIMPLEXA BORDETELLA UNIVERSAL DIRECT CLINICAL AGREEMENT
The performance of the Simplexa Bordetella Universal Direct assay is comparable for either extracted and non-extracted nucleic acid methodology.
Specimen | Sensitivity | Specificity |
Bordetella pertussis | 98.5% | 96.8% |
Bordetella parapertussis | 100% | 98.0% |
Ordering Info
PRODUCT | CODE | REACTIONS |
Simplexa Bordetella Universal Direct | MOL2700 | 100 |
Simplexa Bordetella Universal Direct | MOL2275 | 1000 |
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- Product: Simplexa Bordetella Universal Direct Kit
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