Product Description
Product details
| CAT No : | R0162C |
| Test Type | Rapid Test |
| Brand | CTK BioTech |
| Number of Reactions(Preps)/Kit | 25 |
| Result Time (Rapid Kits) | 15 min |
| Sample Type | Blood |
Individually sealed foil pouches containing:
One cassette device
One desiccant
Stool collection devices, each containing 1 mL Fecal Sample Extraction Buffer (REF SB-R0162)
Sample diluent (REF SB-R0162-2, 5 mL/bottle)
Plastic droppers
Patient ID stickers
One package insert (instruction for use).
Efficient and Reliable Typhoid DetectionThe OnSite S.Typhi Paratyphi Ag Rapid Test delivers accurate detection of typhoid antigens, making it essential for timely diagnosis. Its advanced lateral flow immunoassay technology ensures high sensitivity and specificity, providing peace of mind to healthcare professionals. This rapid, qualitative test operates with silent manual handling, supporting efficient workflows in clinical environments.
Easy-to-Use and Portable DesignEach individually packed cassette is lightweight, requires no specialized instruments, and can be easily used at the patient's side. The simple sample addition and visual interpretation enable clinics and diagnostic centers to conduct the test seamlessly, even in resource-limited settings.
Built-In Safety and Quality ControlsFor enhanced reliability, every cassette includes a procedural control line as part of the test strip, allowing instant internal QC with each use. Lot number tracking and robust packaging help maintain traceability and integrity throughout storage and distribution.
FAQ's of OnSite S.Typhi Paratyphi Ag Rapid Test:
Q: How does the OnSite S.Typhi Paratyphi Ag Rapid Test work?
A: This rapid test employs lateral flow immunoassay technology to detect S. Typhi and S. Paratyphi antigens in whole blood, serum, or plasma. A sample is added to the cassette, and results are visually interpreted within 15 minutes.
Q: What types of samples can be used with this rapid diagnostic kit?
A: The test is compatible with minimally invasive samples, including whole blood, serum, or plasma, allowing flexible use in different clinical settings.
Q: When should the test be used during diagnosis?
A: The test is intended for use whenever rapid typhoid fever detection is required, ideally at the initial clinical assessment in hospitals, labs, or diagnostic centers.
Q: Where can the OnSite S.Typhi Paratyphi Ag Rapid Test be performed?
A: It can be conducted at clinical laboratories, hospitals, diagnostic centers, or in any healthcare setting equipped for blood collection, as no specialized analyzer is needed.
Q: What is the procedure for using the rapid test?
A: Collect the sample (whole blood, serum, or plasma), dispense it onto the cassette using the supplied dropper, and visually interpret the presence or absence of colored lines after 15 minutes.
Q: How do the built-in quality controls benefit users?
A: Every cassette includes a procedural control line to verify the test has functioned correctly, ensuring reliable results without the need for external controls.
Q: What are the main benefits of this rapid test for healthcare providers?
A: Healthcare professionals benefit from its portability, quick turnaround time, accuracy (>95% sensitivity and specificity), minimal equipment requirements, and easy integration into existing diagnostic routines.