
Sample preparation
9. Mix 100 μl of the Assay running buffer, included in the kit (A003), with 10uL fresh isolated plasma sample
in a clean tube by pipetting up and down at least 5 times or vortex briefly.
NOTE: Do not leave the mix for longer than one hour.
10. Transfer 60 μl of the mix to the suPARnostic® Quick Triage device.
11. Place the Lateral Flow cassette in the correct orientation into the drawer, as shown in the figure.
12. Insert the drawer into the device. Touch the “forward” button to proceed and confirm that the cassette
has been inserted in the correct orientation.
13. Read the 2D-barcode with the Patient ID or write the Patient ID manually.
Obtain results
14. The test results will appear on the screen after the test run has finished.
15. Touch the “Print” button to print the results with DYMO LabelWriter or touch the “Export to
USB stick” button to save the data in .csv format on USB.
16. Connect to the hospitals IT system if needed. For further information see the Qiagen User manual QLC
connect (ESLR22-DH-0001 User manual QLC connect 01) or contact Qiagen at
Summary table for sample preparation
1. Transfer 100 µl of running buffer to an empty tube.
2. Transfer 10 µl of plasma sample to the tube containing 100 µl of running buffer.
Vortex the mixture or use the pipet to mix up and down.
3. Transfer 60 μl of the diluted sample to the well of the suPARnostic® Quick Triage device.
4. Scan the suPARnosticQT method barcode. Incubate
the device for 20 min on the table. Insert the device
into the aLF Reader before running the method. (If the
user is NOT present during the incubation it is
recommended to use the suPARnosticQT20 method).
4. Scan the suPARnosticQT20 method barcode.
Insert the device in the aLF Reader for incubation
and touch “forward”to activate the 20 minute
incubation.
5. Press “forward”to read the device with the aLF
Reader. Use the designated batch method.
5. aLF Reader reads the device automatically after
20 min.