Product Description
| Brand | CTK Biotech |
| Sample Type | Serum/ Plasma/ WB |
| Pack Size | 10T |
| CAT No | R0253C |
The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood.
Comprehensive Detection in MinutesThis rapid test enables early and simultaneous screening of multiple TORCH pathogens-Toxoplasma gondii, Rubella, Cytomegalovirus, and Herpes simplex-using just a small blood sample. Results are easy to interpret, appearing as colored visual bands on each panel. Healthcare professionals can confidently obtain results within 15 minutes, ensuring timely clinical decisions.
Ready-to-Use and Simple OperationEach kit is supplied with all necessary components: the test cassette, a dropper, buffer solution, and detailed instructions. There is no need for additional equipment. The manual, real-time procedure requires minimal training and ensures reliability through a built-in control line that confirms the test's validity.
Flexible and Convenient StorageThe OnSite TORCH Panel Rapid Test can be stored at room temperature-between 2C and 30C-without refrigeration or freezing. Its sealed, lightweight packaging makes it easy to transport and deploy in a variety of healthcare settings, such as clinics, hospitals, and laboratories.
FAQ's of CTK Biotech OnSite TORCH Panel Rapid Test:
Q: How is the CTK Biotech OnSite TORCH Panel Rapid Test used?
A: Simply add a drop of serum, plasma, or whole blood to the test device, followed by the buffer solution. Visual lines will appear within 15 minutes to indicate the presence or absence of target antibodies. Detailed instructions are provided in each kit for accurate operation.
Q: What does this rapid test detect?
A: This test is designed for the qualitative detection of IgG and IgM antibodies against Toxoplasma gondii, Rubella virus, Cytomegalovirus, and Herpes simplex virus in human blood samples, allowing for comprehensive TORCH infection screening.
Q: When should the test be performed or results read?
A: The test should be performed at room temperature, following sample collection. Results are visually interpreted exactly 15 minutes after adding the sample and buffer-not before or after that time frame for optimal accuracy.
Q: Where can the OnSite TORCH Panel Rapid Test be used?
A: Its portability and ambient storage capability make it suitable for use in a wide range of settings, including clinics, hospitals, mobile laboratories, and remote locations. The kit does not require power or specialized instruments.
Q: What is the process for disposing of used test kits?
A: Dispose of all used test components as biohazardous waste according to local regulations. Safe handling and disposal are essential to prevent contamination.
Q: What are the main benefits of this rapid test kit?
A: The key benefits include quick, high-accuracy results (>95%), simultaneous detection of multiple pathogens, portability, and ease of use without the need for complicated equipment or refrigeration.