QIAstat-Dx Gastrointestinal Panel 2 Mini B&V – FDA-cleared test to analyze 4 bacterial and 1 viral target for common pathogens causing gastrointestinal symptoms using preserved stool samples (Para-Pak C&S and FecalSwab). This is our targeted seasonal panel, ideal for outpatient testing.
QIAstat-Dx GI Panel 2 Mini B&V – 5 bacterial and viral targets
Bacteria
Viruses
Campylobacter
Salmonella
Shiga-like toxin E. coli (STEC)
Shigella
Norovirus
The QIAstat-Dx GI Panel 2 Mini B&V is available for use on the QIAstat-Dx Analyzer 2.0 and the QIAstat-Dx Rise.
QIAstat-Dx Gastrointestinal Panel 2 Mini B – FDA-cleared test to analyze 5 bacterial targets for common pathogens causing gastrointestinal symptoms using preserved stool samples (Para-Pak C&S and FecalSwab). This is our targeted panel, ideal for outpatient testing.
QIAstat-Dx GI Panel 2 Mini B – 5 bacterial targets
Bacteria
Campylobacter
Salmonella
Shiga-like toxin E. coli (STEC)
Shigella
Yersinia enterocolitica
The QIAstat-Dx GI Panel 2 Mini B is available for use on the QIAstat-Dx Analyzer 2.0 and the QIAstat-Dx Rise.
6 individually packaged cartridges containing all reagents needed for sample preparation and multiplex RT-PCR, plus internal control, including six transfer pipettes.
Features
Intuitive workflow with minimal hands-on time
Uses RT-PCR to deliver comprehensive results in about an hour
Provides Ct values and amplification curves for all detected pathogens directly on the instrument touchscreen
No precision pipetting required
QIAsphere-connected for real-time updates and custom epidemiology reports*
Principle
The QIAstat-Dx Analyzer 2.0, combined with QIAstat-Dx assay cartridges, use real-time PCR to detect pathogen nucleic acids in human biological samples. The QIAstat-Dx Analyzer 2.0 and cartridges are designed as closed systems that contain all necessary reagents, enabling hands-off sample preparation. Detected real-time amplification signals are interpreted by the integrated software and are reported via an intuitive user interface.
Procedure
Setting up and running a QIAstat-Dx test requires minimal hands-on time and just a few simple steps.
Add the patient sample to the main port of the QIAstat-Dx cartridge using the plastic pipette provided. This step is fast and easy to perform and requires no precision pipetting.
Press the Run Test button on the QIAstat-Dx touch screen and scan the sample ID barcode.
Scan the barcode of the cartridge you’re using.
For our QIAstat-Dx Gastrointestinal Panel 2 test, select the sample type (Para-Pak C&S or FecalSwab).
Position the cartridge on the instrument’s sample port. The cartridge will automatically move in and the test will start.
After about an hour, view the comprehensive results.
6 individually packaged cartridges containing all reagents needed for sample preparation and multiplex RT-PCR, plus internal control, including six transfer pipettes.
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QIAstat-Dx GI Panel 2 Mini B
6 individually packaged cartridges containing all reagents needed for sample preparation and multiplex RT-real time PCR, plus internal control, including six transfer pipettes.
QIAstat-Dx instruments and QIAstat-Dx panels are intended for in vitro diagnostic use.
For up-to-date licensing information and product-specific disclaimers, see the respective QIAGEN kit instructions for use or user manual. QIAGEN instructions for use and user manuals are available at www.qiagen.com or can be requested from QIAGEN Technical Services (or your local distributor).
Specifications
Compatible with
QIAstat-Dx Analyzer 1.0 / 2.0 and QIAstat-Dx Rise
