Rota Virus Test: Quick Detection with Rapid Test Device
Rotaviruses are the most common cause of severe diarrheal disease in young children worldwide, leading to significant morbidity and mortality. Quick and accurate detection of rotavirus infections is critical for managing outbreaks, implementing effective treatment plans, and reducing the virus's spread. QL Biotech proudly presents its frontline defense in this ongoing health battle: The Rotavirus Rapid Test Device.
Designed meticulously for simplicity, reliability, and rapid response, our Rotavirus Rapid Test Device is an invaluable tool for healthcare providers. This innovative diagnostic device utilizes state-of-the-art immunochromatographic assay technology to detect rotavirus's presence directly from fecal samples. The principle behind our test is straightforward yet powerful. Upon introducing a fecal sample to the test strip, specific antibodies within the strip react to the presence of rotavirus antigens. This reaction triggers a visible color change, offering clear, visual results that can be interpreted within minutes without the need for specialized laboratory equipment or extensive training.
Our Rotavirus Rapid Test Device stands as a testament to QL Biotech’s commitment to advancing healthcare through innovation. It embodies our dedication to providing accessible, accurate, and swift diagnostic solutions to the healthcare challenges that loom large in our communities. By enabling early detection, our device plays a pivotal role in the timely intervention and management of rotavirus infections, contributing significantly to the mitigation of its impact on public health.
Each device contains a strip with colored conjugates and reactive reagents pre-spreaded at the corresponding regions.
Specimens dilution tube with
buffer
0.1 M Phosphate buffered saline (PBS) and preservative
Disposable pipettes
For watery specimens collection use.
Package insert
For operation instruction.
NOTE:
The intensity of the color in test region (T) may vary depending on the concentration of aimed substances present in the specimen. Therefore, any shade of color in the test region should be considered positive. Besides, the substances level can not be determined by this qualitative test.
Insufficient specimen volume, incorrect operation procedure, or performing expired tests are the most likely reasons for control band failure.
In the realm of pediatric care and beyond, the Rotavirus Rapid Test Device is more than just a diagnostic tool; it is a beacon of hope for millions of families worldwide. Its design is underpinned by rigorous research and development, ensuring that each test conducted meets the highest standards of accuracy and reliability. Our commitment to excellence is unwavering, as is our mission to arm healthcare professionals with the tools they need to combat the challenges posed by rotavirus. With the Rotavirus Rapid Test Device, QL Biotech is at the forefront of the fight against rotavirus, providing a rapid, reliable, and easy-to-use diagnostic solution. It's an essential asset for clinics, hospitals, and medical facilities everywhere, promising a brighter, healthier future for children around the globe. Trust QL Biotech to be your partner in healthcare innovation, as we continue to develop products that address the most pressing medical needs of our time.
PRINCIPLE
It has been designed to detect rotavirus through visual interpretation of color development in the internal strip. The membrane was immobilized with antirotavirus antibodies on the test region. During the test, the specimen is allowed to react with colored anti-rotavirus antibodies colloidal gold conjugates, which were precoated on the sample pad of the test.
The mixture then moves on the membrane by a capillary action, and interact with reagents on the membrane. If there were enough rotavirus in specimens, a colored band will form at the T region of the membrane.
Product Detail
-
Brand: QL
Specimens: : Feces
Reading time：10 minutes.
Pack：20 T
STORAGE: 2‐30°C
KIT COMPONENTS(Device)
- Individually packed test devices
- Specimens dilution tube with buffer
- Disposable pipettes
- Package insert
PROCEDURE
- Bring tests, specimens, buffer and/or controls to room temperature (15-30°C) before use.
1. Specimen collection and pre-treatment:
1) Use the specimen collection container for specimen collection. Best results will be obtained if the assay is performed within 6 hours after collection.
2) For solid specimens: Unscrew and remove the dilution tube applicator. Be careful not to spill or spatter solution from the tube. Collect specimens by inserting the applicator stick into at least 3 different sites of the feces to collect approximately 50 mg of feces (equivalent to 1/4 of a pea).
For liquid specimens: Hold the pipette vertically, aspirate fecal specimens, and then transfer 2 drops (approximately 50 µL) into the specimen collection tube containing the extraction buffer.
3) Place the applicator back into the tube and screw the cap tightly. Be careful not to break the tip of the dilution tube.
4) Shake the specimen collection tube vigorously to mix the specimen and the extraction buffer. Specimens prepared in the specimen collection tube may be stored for 6 months at -20°C if not tested within 1 hour after preparation.
2. Testing
1) Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. To obtain a best result, the assay should be performed within one hour.
2) Using a piece of tissue paper, break the tip of the dilution tube. Hold the tube vertically and dispense 3 drops of solution into the specimen well (S) of the test device.
Avoid trapping air bubbles in the specimen well (S), and do not drop any solution in observation window.
As the test begins to work, you will see color move across the membrane.
3. Wait for the colored band to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.
Note: If the specimen does not migrate (presence of particles), centrifuge the extracted specimens contained in the extraction buffer vial. Collect 80 µL of supernatant, dispense into the specimen well (S) of a new test device and start afresh following the instructions mentioned above.
KIT COMPONENTS(Device)
Each device contains a strip with colored conjugates and reactive reagents pre-spreaded at the corresponding regions.
Specimens dilution tube with
buffer
0.1 M Phosphate buffered saline (PBS) and preservative
Disposable pipettes
For watery specimens collection use.
Package insert
For operation instruction.
NOTE:
The intensity of the color in test region (T) may vary depending on the concentration of aimed substances present in the specimen. Therefore, any shade of color in the test region should be considered positive. Besides, the substances level can not be determined by this qualitative test.
Insufficient specimen volume, incorrect operation procedure, or performing expired tests are the most likely reasons for control band failure.
In the realm of pediatric care and beyond, the Rotavirus Rapid Test Device is more than just a diagnostic tool; it is a beacon of hope for millions of families worldwide. Its design is underpinned by rigorous research and development, ensuring that each test conducted meets the highest standards of accuracy and reliability. Our commitment to excellence is unwavering, as is our mission to arm healthcare professionals with the tools they need to combat the challenges posed by rotavirus. With the Rotavirus Rapid Test Device, QL Biotech is at the forefront of the fight against rotavirus, providing a rapid, reliable, and easy-to-use diagnostic solution. It's an essential asset for clinics, hospitals, and medical facilities everywhere, promising a brighter, healthier future for children around the globe. Trust QL Biotech to be your partner in healthcare innovation, as we continue to develop products that address the most pressing medical needs of our time.