Product Description
STANDARD F Chikungunya IgM/IgG FIA qualitatively analyzes Chikungunya virus specific IgM and IgG antibodies in serum, plasma and whole blood using fluorescent immunoassay. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.Advantage - Able to perform qualitative analysis with high sensitivity and specificity by using fluorescent substance
- Objective result - Eliminates the subjectivity of a visual result
- Automatic strip recognition by reading the information stored in 2D barcode
Technical Details 
Reliable Chikungunya DetectionThis rapid FIA test kit ensures prompt identification of Chikungunya infection through strong accuracy and sensitivity. By detecting IgM and IgG antibodies, healthcare professionals can distinguish between current and past infections, facilitating well-informed clinical decisions for patient care. Its 15-minute operational time is particularly valuable in settings requiring swift diagnosis.
Efficient Workflow and User-Friendly DesignEach kit is designed for ease of use, providing all essential components including sample pipettes and buffers, pre-measured for accuracy. Instructions are included to ensure correct processes are followed. The kit supports efficient workflows within clinical and laboratory environments, thanks to its simple setup and automatic processing through the STANDARD F Analyzer.
Storage and Portability ConvenienceThe kit is compact (approx. 200 x 150 x 70 mm, 500 grams), portable, and stable for up to 18 months when maintained at 2C to 30C, away from direct sunlight. This allows for flexible storage and handling in diverse laboratory and clinical setups across India, ensuring availability when needed.
FAQ's of STANDARD F Chikungunya IgM/IgG FIA test kit:
Q: How is the STANDARD F Chikungunya IgM/IgG FIA test performed?
A: To perform the test, collect a serum or plasma sample from the patient, add the sample and buffer to the test device, and insert it into the STANDARD F Analyzer. The analyzer will automatically process the reaction and provide results within approximately 15 minutes.
Q: What types of samples can be used with this test kit?
A: The test kit is compatible with human serum or plasma samples. Whole blood and other body fluids are not recommended for this particular assay.
Q: When should this kit be used for Chikungunya diagnosis?
A: This kit is intended for professional laboratory or clinical settings where rapid detection of Chikungunya IgM and IgG antibodies is needed. It is used to support diagnosis during acute or convalescent phases based on antibody response.
Q: Where can I use the STANDARD F Chikungunya IgM/IgG FIA test kit?
A: The kit is designed for use in hospitals, diagnostic laboratories, and clinical research settings. It is not intended for home or self-testing, and must be operated by trained professionals.
Q: What is the process of reading test results with this kit?
A: After the sample and buffer are loaded into the test device, insert the device into the STANDARD F Analyzer. The analyzer interprets the fluorescence signals and displays a qualitative result (positive or negative) on its screen.
Q: What are the main benefits of using this test kit?
A: The main benefits include rapid turnaround (about 15 minutes), high sensitivity and specificity, ease of use, and compatibility with fully automated analyzer systems for consistent, reliable results.
Q: How should the test kit be stored and what is its shelf life?
A: Store the kit at 2C to 30C and keep it away from direct sunlight. The test kit remains stable and effective for up to 18 months from the manufacturing date, as marked on the packaging.