Acon FIAflex PCT FIA Test

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Product Details:

Accuracy 95%
Storage Instructions Store at 2-30C, avoid direct sunlight
Display Type As per analyzer display
Usage Type Diagnostic Laboratory Use
Measurement Range 0.1-100 ng/mL
Function Quantitative measurement of PCT
Shelf Life 12 months from manufacturing
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Acon FIAflex PCT FIA Test Price And Quantity

Acon FIAflex PCT FIA Test Product Specifications

Instruments Type In-vitro Diagnostic Kit
Technology Fluorescence Immunoassay (FIA)
Weight Lightweight
Shelf Life 12 months from manufacturing
Portable Yes
Equipment Type Procalcitonin (PCT) FIA Test
Function Quantitative measurement of PCT
Material High-quality plastic, reagents and buffer solutions
Condition New
Noise Level Silent Operation
Power Consumption Low
Features Rapid result, high sensitivity and specificity, easy to use, compatible with FIAflex Analyzer
Voltage Standard - as per analyzer
Power Source Electric
Display Type As per analyzer display
Storage Instructions Store at 2-30C, avoid direct sunlight
Accuracy 95%
Color White/Blue
Measurement Range 0.1-100 ng/mL
Wall Mounted No
Usage Type Diagnostic Laboratory Use
Use Quantitative detection of Procalcitonin (PCT) in human serum or plasma
Operating Type Automated
Real-Time Operation Yes
Dimension (L*W*H) As per kit box specifications

Transportation Condition Ambient temperature
Regulatory Status IVD CE Marked
Sample Type Human serum or plasma
Sample Volume 100 µL
LOT Number/Batch Number Available on packaging
Kit Contents Test cartridges, buffer solution, pipette, instruction manual
Analyzer Compatibility Designed for use with FIAflex Analyzer
Expected Results Time Within 15 minutes

Product Description

Brand Acon

Sample Type Serum/ Plasma/ WB

Pack Size 25T

CAT No F131-50211

Biomarker Infection

The PCT FIA Test is a fluorescence immunoassay that is used with the FIAflex Fluorescent Immunoassay Analyzer for the quantitative detection of Procalcitonin (PCT) in human serum, plasma, venous whole blood and fingertip blood, which is useful in diagnosis of severe bacterial infection and sepsis.

Advanced PCT Quantification in Minutes

Acon FIAflex PCT FIA Test delivers reliable Procalcitonin quantification in human serum or plasma within 15 minutes. Utilizing Fluorescence Immunoassay technology, this kit ensures high sensitivity and specificity, making it an essential tool for rapid diagnostics in medical laboratories. The streamlined protocol and user-friendly format help labs boost testing efficiency and accuracy.

User-Friendly, Automated Workflow

The kit is designed for easy operation with automated features when paired with the FIAflex Analyzer. Each kit contains clearly labeled test cartridges, buffer solution, a pipette, and a comprehensive instruction manual, enabling fast setup and consistent results. Its compact, lightweight build and ambient temperature stability support straightforward transportation and storage.

FAQ's of Acon FIAflex PCT FIA Test:

Q: How is the Acon FIAflex PCT FIA Test performed?

A: The test involves adding 100 L of human serum or plasma sample to the provided test cartridge, mixing with buffer solution, and processing the cartridge in the FIAflex Analyzer. Results are displayed on the analyzer screen within 15 minutes.

Q: What are the benefits of using this test in diagnostic laboratories?

A: This test offers rapid turnaround, high accuracy (95%), and a measurement range of 0.1-100 ng/mL. Its automated workflow reduces manual handling errors, while its portable and silent design enhances laboratory convenience.

Q: When can I expect to receive test results after sample preparation?

A: You can expect to receive quantitative results within 15 minutes after loading the sample into the FIAflex Analyzer, ensuring timely decision-making for clinicians.

Q: Where should the test kit be stored prior to use?

A: Store the kit between 2C and 30C, avoiding direct sunlight. Its stability at ambient temperatures allows for convenient storage and transportation without compromising performance.

Q: What sample types are compatible with this test?

A: The kit is validated for use with human serum or plasma samples only, supporting quantitative analysis of Procalcitonin levels for clinical diagnostics.

Q: What is included in the test kit package?

A: Each kit contains test cartridges, buffer solution, a pipette, and a user instruction manual to guide you through the analysis process seamlessly.

Q: How does this test support accurate diagnosis?

A: Utilizing advanced FIA technology, the test achieves high sensitivity and specificity, providing clinicians with reliable data for the assessment of bacterial infections or sepsis.

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