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Can the PyroTec™ PRO System be utilized with the PyroGene™ rFC Assay?

The basic system is supplied with Sunrise Readers and supports both the Lonza Kinetic-QCL™ Kinetic Chromogenic LAL Assay (for example, P/N 50-650H) and the PYROGENT™-5000 Kinetic Turbidimetric LAL Assay (for example, P/N N688). The PyroGene™...

PyroTec Pro: Has any stability testing been performed for the endotoxin and lysate that stay on the instrument before use?

Our data indicate that the reagents should be placed on the deck prior to running the automated assay. This would be similar to the methodology when performing the assay on the bench. Customers should follow procedures similar to those in a manual...

How does the PyroTec™ PRO System mix samples after sample dilution?

All mixing on the system is done by the liquid handling robotic arm described above using similar multiple aspiration/dispense steps to those used in standard preparation. The volume for mixing and speed of pipetting is defined in the software and we...

PyroTec Pro: How long does the assay take, and can an assay be run overnight?

Typical runtime from start of the automated microplate setup to completion of WinKQCL™ Software reading the plate for a single assay is 1.5 hours – 2.5 hours, depending on the number of samples and the complexity of the dilutions. Therefore, a...

Are all of the PyroTec Pro consumables endotoxin-free?

All consumables, including pipette tips (P/N 0000229884), troughs (P/N 0000229888), 13 x 100 mm tubes (P/N N207), and microplates (P/N 25-340) used in the system are certified to be endotoxin-free (<0.005 EU/mL).

How long does it take to perform the PyroTec Pro installation, operational and performance (IOPQ)?

There are many components that need to be installed and validated. Depending on the customizations needed, estimated time for installation and operational qualification is one week.

How are PyroTec™ Pro manual steps controlled by WinKQCL software?

Pop-up windows in the WinKQCL™ Software application guide the user through manual preparation (endotoxin, reagents, sample), and every step has to be actively confirmed by the user, which acts as a fail-safe. For data integrity purposes, it reduces...

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