Product Description
Brand: Wondfo
Sample Type: Serum/ Plasma
Pack Size: 25T
CAT No: W282P0001
Biomarker: Infection
The Finecare Dengue NS1 Ag Test is a fluorescence immunoassay used along with Finecare FIA Meters for qualitative detection of Dengue NS1 antigen in whole blood, serum or plasma specimen. It is useful as an aid in screening of early Dengue virus infection.
Rapid and Accurate Dengue DetectionThe Wondfo Finecare Dengue NS1 Ag Test offers fast and precise identification of dengue virus NS1 antigen in serum or plasma samples, with results available in just 15-20 minutes. This test utilizes advanced lateral flow immunoassay technology, ensuring high sensitivity and specificity for early disease detection. Its single-use, instrument-free format makes it suitable for a variety of clinical environments, from hospitals to field clinics.
User-Friendly and Instrument-FreeDesigned for straightforward operation, the test requires no specialized equipment. Medical professionals simply apply the sample and buffer to the cassette and visually interpret the results, minimizing training needs and allowing for rapid deployment. The kit's portability and manual operation mean it can be used in both urban and remote locations with confidence.
FAQ's of Wondfo Finecare Dengue NS1 Ag Test:
Q: How is the Wondfo Finecare Dengue NS1 Ag Test performed and interpreted?
A: To perform the test, collect a serum or plasma sample and apply it to the cassette along with the provided buffer. Wait 15-20 minutes, then interpret the results visually based on line appearance as indicated in the instructions.
Q: What are the benefits of using this Dengue rapid test kit?
A: The kit provides early, accurate dengue detection with over 95% accuracy, rapid results in under 20 minutes, and requires no instruments, making it ideal for hospitals, clinics, and field use. It is highly portable, easy to use, and reliable.
Q: When should this test be used in patient management?
A: This test is intended for use during the early stages of dengue infection, as it detects the NS1 antigen present in the first days of symptom onset. Early diagnosis facilitates prompt clinical intervention.
Q: Where can the test be used, and who is it intended for?
A: It is designed for professional in vitro diagnostic use in medical laboratories, hospitals, clinics, and by healthcare providers in India involved in dengue surveillance and management. It is not intended for home use or self-testing.
Q: What are the storage conditions for maintaining test accuracy?
A: Kits must be stored between 2C and 30C in their original sealed packaging. Exposure to direct sunlight or temperatures outside this range may compromise test performance.
Q: What makes the Wondfo Finecare test easy to use for professionals?
A: The test is supplied in a ready-to-use plastic cassette format with an accompanying buffer. No additional instruments or special equipment are required, and a straightforward manual process reduces the likelihood of user error.