Product Description
- BrandCTK Biotech
- Sample TypeSerum/ Plasma/ WB
- Pack Size30T
- CAT NoR0066C
The OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood.
Quick and Reliable Chikungunya DetectionAchieve rapid Chikungunya screening with results in just 10-15 minutes. Designed specifically for qualitative detection of IgM antibodies, the OnSite Chikungunya IgM Combo Rapid Test simplifies the diagnosis process for healthcare facilities, ensuring timely decisions for patient care.
Simple Usage, No Special Equipment RequiredThis rapid test features an easy, one-step procedure that requires minimal training and no advanced laboratory devices. Just add the sample and buffer to the cassette-the clear visual indicator lines will reveal results quickly and efficiently.
Versatile Sampling and High AccuracyCompatible with whole blood, serum, or plasma samples, the test delivers excellent sensitivity and specificity (>98%). Its flexibility and high accuracy make it an essential tool for healthcare professionals managing suspected Chikungunya cases.
Convenient and Portable for Point-of-CareHoused in a compact plastic cassette, each test is lightweight and portable, making it ideal for on-site testing anywhere clinical decisions are needed. With built-in procedural control lines, confidence in results is ensured every time.
FAQ's of CTK Biotech OnSite Chikungunya IgM Combo Rapid Test:
Q: How do I perform the CTK Biotech OnSite Chikungunya IgM Combo Rapid Test?
A: To use the test, add either 10 L of serum/plasma or 20 L of whole blood to the sample well, followed by the provided buffer solution. Wait 10-15 minutes, and then interpret the colored indicator lines for a qualitative result.
Q: What types of samples can be used with this test kit?
A: The rapid test is compatible with human whole blood, serum, or plasma, providing flexibility in sample collection based on your clinical setting.
Q: When should I use this test for Chikungunya detection?
A: The test is intended for professional use whenever there is a need to screen for recent or acute Chikungunya virus infection, especially in symptomatic patients or outbreak investigations in clinics, hospitals, or point-of-care settings.
Q: What is the benefit of using this rapid test over traditional laboratory testing?
A: This rapid test offers high accuracy (sensitivity and specificity both over 98%) as well as immediate results within 15 minutes-no need for specialized laboratory equipment, enabling quick decisions and timely patient management.
Q: Where can the test be performed and who can use it?
A: The test is designed for use by trained healthcare professionals in medical settings such as clinics, hospitals, and laboratories throughout the United States.
Q: What controls are built into the test kit to ensure accuracy?
A: Each test cassette contains a built-in procedural control line. This ensures proper function and verifies that the test was performed correctly. If the control line does not appear, the result is invalid and should not be interpreted.
Q: How should the test kits be stored and what is their shelf life?
A: Store the kits at 2-30C, avoid direct sunlight, and do not freeze. Each test is good for single use only and maintains its efficacy for 24 months from the date of manufacture, as indicated on the package label.