- Seasonal Influenza A/H1
- Seasonal Influenza A/H3
- 2009 H1N1 Influenza
Results in as little as 4 hours
ProFAST+ uses proven real-time PCR technology, ensuring that accurate test results are delivered quickly and easily. The test's compatibility with automated nucleic-acid extraction technology minimizes hands-on time and expedites results. All the ingredients you need, except water, are included in the kit.
Easy to use and implement in the lab
Designed to run on standard molecular diagnostic equipment, ProFAST+ has a simple workflow that makes it easy to implement and validate. A common RNA Internal Control allows a single nucleic-acid extract to be used in any combination of Prodesse's respiratory RNA virus Assays.
|ProFAST+ Detection Kit
An easy-to-use real-time multiplex RT-PCR kit for Influenza A that discriminates: Seasonal A/H1, Seasonal A/H3, and 2009 H1N1
|Cat #||Product||Kit Size||PI|
|H34VK00||ProFAST+ Detection Kit||100||EN FR DE IT ES|
|Cat #||Product||Kit Size||MSDS|
|H34VK00||ProFAST+ Detection Kit||100||HSM34 EN DE ES FR IT
HCT34 EN DE ES FR IT
GLS26 EN DE ES FR IT
GLS33 EN DE ES FR IT
GCT12 EN DE ES FR IT
The ProFAST+ assay was cleared for In Vitro Diagnostic Use by the FDA in 2010 and is licensed by Health Canada. The ProFAST+ assay is CE marked for In Vitro Diagnostic Use.
For additional availability in other countries please contact your local sales rep or distributor.
Prospective Data from Clinical Trials
Please see package insert for detailed information.