Product Description
| Brand | CTK Biotech |
| Sample Type | Serum/ Plasma/ WB |
| Pack Size | 10T |
| CAT No | R0095C |
A lateral flow chromatographic immunoassay for the qualitative detection of IgM antibodies to hepatitis E virus (HEV) in human serum or plasma.
Reliable HEV IgM Detection for ProfessionalsCTK Biotech's Onsite HEV IgM Rapid Test is intended for professional use, providing dependable identification of IgM antibodies for Hepatitis E Virus in human serum or plasma. Designed with a robust lateral flow immunoassay, the kit emphasizes accuracy and speed, enhancing efficiency in clinical decision-making.
Effortless Operation, Rapid ResultsWith a simple manual process and visual readout, this test delivers clear results in just 10-15 minutes. The included components require no additional equipment, making the kit easy to use and perfectly suited for rapid diagnostics in a variety of healthcare settings.
Portability and Long Shelf LifeEach lightweight and compact test cassette is single-use and straightforward to transport, ideal for onsite or field applications. With a shelf life of 18 months from the manufacturing date and recommended storage between 2-30C, the kit assures readiness and reliability whenever needed.
FAQ's of CTK Biotech Onsite HEV IgM Rapid Test CE:
Q: How does the CTK Biotech Onsite HEV IgM Rapid Test function?
A: The test utilizes a lateral flow immunoassay technique, detecting the presence of IgM antibodies specific to Hepatitis E Virus. When serum or plasma is applied, any HEV IgM antibodies react with specific reagents on the test line, producing a visually detectable colored line.
Q: What samples are needed to perform this test?
A: The HEV IgM Rapid Test requires either human serum or plasma samples for accurate detection, as specified in the kit instructions.
Q: When and where should the test be used?
A: This diagnostic kit is intended for use by trained healthcare professionals in clinical settings, laboratories, or field medical operations where rapid HEV IgM antibody detection is essential.
Q: What is the procedure for conducting the test?
A: After collecting the required serum or plasma sample, a few drops are applied to the test cassette using the provided dropper. The buffer is then added, and results can be visually read after 10-15 minutes by observing colored lines on the cassette.
Q: How accurate and reliable is the test?
A: According to the manufacturer, the test demonstrates greater than 99% accuracy for HEV IgM detection. The cassette includes a built-in procedural control line to confirm the test is functioning properly.
Q: What are the key benefits of using this test kit?
A: The kit offers rapid results, portability, single-use convenience, high sensitivity and specificity, and compliance with CE standards, making it invaluable for timely Hepatitis E diagnosis.