Product Description
STANDARD F PCT FIA is a fluorescent immunoassay for the quantitative measurement of procalcitonin level in human serum, plasma, and whole blood. Procalcitonin helps assess the severity and prognosis of bacterial infections, and support early diagnosis of sepsis.Advantage
- Fluorescent technology- Optimized performance
- Reagents can be stored at room temperature
- No-coding via 2D barcode system
Advanced Fluorescent TechnologyThe STANDARD F PCT FIA test kit employs sandwich immunodetection based on fluorescent technology, ensuring rapid and highly sensitive results. This innovative approach enables reliable quantification of Procalcitonin levels, supporting clinicians in making informed decisions efficiently within minutes.
Easy Operation, Precise ResultsDesigned for professional use, the kit requires only 75 L of sample and minimal manual preparation. The result is automatically read by the compatible STANDARD F Analyzer, eliminating subjectivity and providing accurate measurements every time. The process is streamlined for both laboratory and point-of-care applications.
Comprehensive Kit for Professional SettingsThis product includes 25 test devices, sample tubes, dropper tips, buffer solution, an ID chip, and a package insert, making it ready to use out of the box. All components meet medical grade standards, and detailed instructions ensure simple yet effective operation in various clinical environments.
FAQ's of STANDARD F PCT FIA test kit:
Q: How does the STANDARD F PCT FIA test kit work?
A: The test kit uses sandwich immunodetection with fluorescent technology to detect and quantify Procalcitonin (PCT) in serum, plasma, or whole blood samples. After adding the sample and reagents, the STANDARD F Analyzer reads the fluorescence signal and calculates PCT concentration within 15 minutes.
Q: What is the intended use of this PCT test kit?
A: This kit is intended for in-vitro quantitative detection of Procalcitonin (PCT) as a rapid aid in diagnosing bacterial infections and sepsis, primarily for use by laboratory professionals and healthcare practitioners in professional or point-of-care settings.
Q: What sample types and volume are required for testing?
A: The kit is compatible with serum, plasma, and whole blood samples. For each test, a sample volume of 75 L is required.
Q: How soon are results available and how are they interpreted?
A: Results are available within 15 minutes and are interpreted instrumentally using the STANDARD F Analyzer. The analyzer automatically displays quantitative results on its screen, eliminating manual interpretation.
Q: What are the storage requirements for the kit and opened cassettes?
A: The kit should be stored at 2-30C, kept away from direct sunlight, and should not be frozen. Test cassettes must be used immediately after opening, ideally within one hour, to ensure result accuracy.
Q: Where can the STANDARD F PCT FIA test kit be used?
A: This kit is suitable for professional environments including laboratories and point-of-care settings. It is not intended for home or self-use, as operation and interpretation require compatible instrumentation and professional expertise.
Q: What are the main benefits of using this test kit?
A: Benefits include rapid turnaround time (results within 15 minutes), high sensitivity and accuracy (95%), minimal sample required, and simple handling. The automated analyzer reading ensures precise and objective results for better patient management.