Product Description
| Brand | CTK Biotech |
| Sample Type | Serum/ Plasma/ WB |
| Pack Size | 10T |
| CAT No | R0090C |
Individually sealed foil pouches containing: One cassette device One desiccant 5 L capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use)
Efficient Detection of Acute HAV InfectionsThe OnSite HAV IgM Rapid Test offers a fast, reliable means to detect HAV IgM antibodies, indicating recent Hepatitis A virus infection. Utilizing a simple manual process, healthcare professionals can identify antibodies in serum, plasma, or whole blood with ease. Its high sensitivity and specificity facilitate timely diagnosis and management of patients.
Simple, Portable, and Ready for UseDesigned for straightforward operation, this test requires only a small sample volume and produces visual colored lines for easy result interpretation. Its portable format enables use in various clinical environments, including remote or resource-limited settings, without the need for specialized laboratory equipment.
Supplied Complete and conveniently PackagedEach kit is individually packaged with essential materials: a test cassette, sample dropper, desiccant, and thorough instructions. The tests remain stable for up to 24 months when stored properly, ensuring availability and reliability whenever needed. Single-use design enhances infection control and test consistency.
FAQ's of CTK Biotech OnSite HAV IgM Rapid Test:
Q: How do I use the CTK Biotech OnSite HAV IgM Rapid Test?
A: To use the test, collect 10 L of serum/plasma or 20 L of whole blood, add it to the sample well of the cassette using the provided dropper, and then add the buffer as instructed. Wait approximately 15 minutes to visually interpret the appearance of colored lines for results.
Q: What sample types are compatible with this test kit?
A: The test is validated for use with human serum, plasma, or whole blood samples, giving flexibility in various clinical and laboratory settings.
Q: When can this test be performed following suspected exposure to Hepatitis A?
A: The test detects IgM antibodies, which typically appear during the acute phase of infection. Testing is appropriate when a recent or current Hepatitis A infection is clinically suspected.
Q: Where can this rapid test be used?
A: Thanks to its portable design and silent, manual operation, the test is suitable for hospitals, clinics, field settings, community health centers, and other point-of-care environments.
Q: What is the benefit of using this rapid test kit over traditional laboratory tests?
A: This kit delivers qualitative results in about 15 minutes without the need for additional equipment, making it ideal for rapid decision-making and improving patient management, particularly in settings lacking conventional laboratory infrastructure.
Q: What are the storage requirements for the kit?
A: Store the kit at temperatures between 2C and 30C inside the original sealed pouch. Avoid freezing to maintain performance throughout the kit's 24-month shelf life.
Q: Is the test reusable, and how should it be disposed of after use?
A: Each test is single-use only. After use, the kit and any components should be disposed of as per standard biohazard waste management protocols.