Product Description
Brand Mindray
Sample Type Serum
Pack Size 2 x 50T, 2 x 100T
CAT No 10500422800, 10500425500
Application Immuno-Assay
Ourchemiluminescence immunoassay reagentshave been specially developed to work with Mindray's CL series automatic chemiluminescence immunoassay analyzers to make a complete system, offering high reliability and accuracy. Mindray uses liquid, ready-to-use reagents which come in two packages, 50 tests and 100 tests, to suit customers with different requirements.
Advanced CLIA Technology for Accurate ResultsHarnessing chemiluminescence immunoassay (CLIA) technology, the Mindray Progesterone kit enables highly sensitive and specific detection of progesterone in clinical samples. This quantitative method provides precise data essential for diagnostics, with built-in controls guaranteeing result reliability. Each ready-to-use kit is manufactured under stringent quality conditions, supporting robust laboratory workflows.
Seamless Integration and Ease of UseThe kit is tailored for Mindray CL-series analyzers, ensuring seamless integration into existing laboratory systems. Detailed instructions and barcode labeling simplify inventory and test setup, while automatic operation on compatible instruments helps minimize user intervention. All reagents are pre-measured and supplied in a convenient white/blue box, optimizing efficiency for clinical laboratories.
FAQ's of Mindray Progesterone (CLIA):
Q: How is the Mindray Progesterone (CLIA) test performed in the laboratory?
A: The test is carried out on compatible Mindray CL-series analyzers, using an automatic process based on the sandwich chemiluminescence immunoassay principle. Human serum or plasma samples are processed with the kit's pre-dispensed reagents as described in the included Instruction for Use (IFU).
Q: What samples are suitable for the Mindray Progesterone (CLIA) kit?
A: This kit is designed for use with human serum or plasma samples. It is intended for professional in-vitro diagnostic application within clinical or laboratory settings.
Q: When should the calibration and controls be performed during testing?
A: Calibration should be performed according to your instrument's protocol as outlined in the IFU. Internal controls are included in the kit and should be run as specified to ensure the accuracy and validity of test results.
Q: Where can I find critical information like expiry dates and lot numbers?
A: The expiry date is labeled directly on the outside of the kit box, while the lot number is indicated on the kit's packaging. For added traceability, a barcode is also present on the packaging.
Q: What are the storage requirements for the Mindray Progesterone (CLIA) kit?
A: The kit must be stored at 2-8C and should not be frozen. Always refer to the box for the stated expiration date, which is typically 12-18 months from the date of manufacture.
Q: What are the key benefits of using this kit in the laboratory?
A: This kit provides high specificity and sensitivity through advanced CLIA technology. It features ready-to-use reagents, integrated controls, and supports automated, real-time operation when used on Mindray CL-series analyzers, ensuring precise and efficient workflow in diagnostic settings.