STERGIC HCV AB Rapid Test 1's
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The Stergic HCV AB Rapid Test kit offers a convenient method for the qualitative detection of antibodies to the Hepatitis C Virus. It is designed for professional use in healthcare facilities, clinics, and laboratories to aid in the diagnosis of individuals who may be at risk of Hepatitis C infection. This test utilizes a chromatographic immunoassay to detect HCV antibodies in serum, plasma, or whole blood samples, providing a preliminary result.
Rapid Results: The test provides results within a 15-20 minute timeframe, allowing for swift processing in clinical settings. High Sensitivity: It is designed to detect even low concentrations of HCV antibodies, which can aid in early detection. User-Friendly Design: The kit includes a simple procedure with straightforward instructions, making it accessible for healthcare professionals. Versatile Specimen Collection: The test can be performed using serum, plasma, or whole blood samples. For Professional Use: This diagnostic tool is intended for use by healthcare professionals in laboratory or near-patient environments.
Q: Is the STERGIC HCV AB Rapid Test for home use?
A: This test is designed for in-vitro diagnostic use and is suitable for healthcare facilities, clinics, and laboratories. It is intended for use by healthcare professionals.
Q: What does this test detect?
A: This is a screening test that qualitatively detects the presence of antibodies to the Hepatitis C Virus (HCV) in human serum, plasma, or whole blood.
Q: How long does it take to get the results?
A: The results of the test are typically available within 15 to 20 minutes after performing the procedure.
Q: What should I do if the test result is positive?
A: A positive result indicates that you may have been exposed to the Hepatitis C virus. It is not a confirmatory diagnosis. You must consult a healthcare professional for further evaluation, confirmatory testing, and medical guidance.
Q: What kind of sample is required for the test?
A: The test can be performed using a sample of whole blood, serum, or plasma. The collection should be done carefully to avoid contamination.
This test kit is a tool for the preliminary screening of Hepatitis C. Its main purpose is to detect the presence of HCV antibodies, which can assist healthcare professionals in making an initial assessment.
1. Collect a whole blood, serum, or plasma sample as per standard clinical procedures. 2. Apply the collected sample to the designated area on the test cassette. 3. Add the provided buffer solution as directed in the kit's instructions. 4. Wait for the specified time, typically 15-20 minutes, to read the results. 5. Interpret the results according to the appearance of lines in the control and test regions, as explained in the instruction manual.
This product is intended for in-vitro diagnostic use only. It is designed for single use and should not be reused. Store the test kit in a cool, dry place, away from direct sunlight. Wear appropriate protective equipment, such as gloves and eye protection, when handling samples and performing the test. A positive result requires further confirmatory testing and medical evaluation by a healthcare professional. The test should not be used for self-testing or for screening blood donations. Dispose of the used test kit and materials according to local regulations for biohazardous waste.
The test provides a preliminary, qualitative result. The presence of a colored line in the control region indicates the test is valid, while the presence of a line in the test region indicates a reactive result for HCV antibodies. An absence of the control line means the test is invalid and should be repeated.
The contents of this website are for informational purposes only and not intended to be a substitute for professional medical advice, diagnosis, or treatment. Please seek the advice of a physician or other qualified health provider with any questions you may have regarding a medical condition. Do not disregard professional medical advice or delay in seeking it because of something you have read on this website.
