Product Description
AFP (Alpha Fetal Protein) Rapid Quantitative Test:-The Finecare AFP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare FIA System for quantitative determination of Alpha-Fetoprotein in human whole blood, serum or plasma. The test is used as an aid for early auxiliary diagnosis and the evaluation of therapeutic efficiency for primary hepatic carcinoma.
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STORAGE AND STABILITY1. Store the test kit at 430 up to the expiration date printed on package.
2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing.
3. Do not remove the Test Cartridge from the pouch until use. The Test Cartridge should be used within 1 hour once opened.
Why Choose Finecare AFP Test Kit?The Finecare AFP Test Kit combines state-of-the-art technology with simple, manual operation to provide fast and accurate results for AFP quantification in blood samples. Its design makes it suitable for a range of diagnostic settings, enhancing early detection and effective monitoring of liver-related diseases.
Rapid and Reliable TestingWith a turnaround time of just 15 minutes and measurement range from 0.5 to 1000 ng/mL, this kit supports real-time clinical decisions. Its lateral flow immunofluorescence assay ensures top-tier accuracy and sensitivity, pivotal for patient management and disease surveillance.
User-Friendly and PortableWeighing approximately 200 grams and featuring straightforward sample preparation, the kit is easy to transport between clinical settings. Its intuitive manual operation makes it accessible to a wide range of healthcare professionals, streamlining workflow without compromising reliability.
FAQ's of Finecare AFP Test Kit:
Q: How is the Finecare AFP Test Kit used for AFP detection?
A: The kit is used to quantitatively detect Alpha-Fetoprotein (AFP) in human serum, plasma, or whole blood by following instructions in the manual. After applying a 75 L sample to the test cassette with the provided dropper and buffer, results are read within 15 minutes using the Finecare FIA Meter.
Q: What benefits does this test kit offer for early liver cancer detection?
A: The Finecare AFP Test Kit enables rapid and sensitive identification of elevated AFP levels, which are associated with liver cancer and other related conditions. Its swift results can support early diagnosis and timely treatment interventions, possibly improving patient outcomes.
Q: When should the Finecare AFP Test Kit be used?
A: This test kit is ideal for early detection of liver cancer, monitoring treatment progress, and assisting diagnosis of AFP-related disorders in clinical laboratories, hospitals, and diagnostic centers. It should be used whenever quantitative AFP analysis is required.
Q: Where can this test kit be deployed?
A: Due to its portability and user-friendly design, the kit can be utilized in various settings including clinical laboratories, hospitals, and diagnostic centers. It is suitable for both stationary and mobile diagnostic environments.
Q: What is the process for storing and handling the Finecare AFP Test Kit?
A: For optimum performance, store the kit at 2-30C while keeping it away from sunlight and moisture. Ensure that components remain sealed until use, and follow the provided instruction manual for accurate results.
Q: What makes the Finecare AFP Test Kit highly sensitive and accurate?
A: This kit employs lateral flow immunofluorescence assay technology, delivering results with over 95% accuracy and a broad measurement range. Its design ensures precise quantification of AFP, supporting reliable clinical diagnostics.
Q: Is the Finecare AFP Test Kit suitable for real-time diagnostic operations?
A: Yes, the kit provides real-time operation with rapid result generation, empowering healthcare professionals to make timely decisions during patient diagnosis and monitoring.