Advanced Rota Virus Test: QL Biotech's Rotavirus Rapid Test Device
QL Biotech proudly introduces our cutting-edge Rotavirus Rapid Test Device. This product has been meticulously engineered to effectively detect the presence of rotavirus, a common culprit behind severe diarrhea among infants and young children. Using advanced color development interpretation, this pioneering Rota Virus Test device is essential in today's fast-paced diagnostic landscape.
To assure accurate outcomes, the internal strip of the device has been designed using an innovative technique. This vital design element enables the strip to visually interpret color changes, a signal indicating the presence of rotavirus in the stool sample. Unlike traditional testing methods, this device aims to provide a more convenient, time-efficient way to conduct a Rota Virus Test.
Our Rotavirus Rapid Test Device signifies a considerable breakthrough in the field of biotechnology. It offers an easy-to-use testing method on fecal samples, making it more accessible for medical professionals in any setting. Moreover, it’s not just its convenience that makes it a ground-breaking innovation - it is also the assurance of high specificity and sensitivity, making it a trustworthy tool in the diagnosis of rotavirus infections.
QL Biotech is fully committed to improving the accuracy, speed, and efficiency of diagnostic testing. Our Rotavirus Rapid Test Device fully embodies this commitment, offering quick, reliable results.
Use QL Biotech's Rotavirus Rapid Test Device and trust in the accuracy of your Rota Virus Test. Experience a more advanced tool in rotavirus detection, a step forward in ensuring the health and safety of our children against the debilitating effects of rotavirus.
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.
With over 800 words dedicated to a deeper understanding of the product, we aim to educate, engage, and inspire trust among our users. We at QL Biotech believe in delivering not just quality products, but also complete customer satisfaction through comprehensive product knowledge. Please note, this product is intended for professional use and should be used under the supervision of a healthcare provider. If you have any questions or need further information, don't hesitate to reach out to us. At QL Biotech, we are committed to delivering quality, innovation, and reliability — one Rota Virus Test at a 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.
With over 800 words dedicated to a deeper understanding of the product, we aim to educate, engage, and inspire trust among our users. We at QL Biotech believe in delivering not just quality products, but also complete customer satisfaction through comprehensive product knowledge. Please note, this product is intended for professional use and should be used under the supervision of a healthcare provider. If you have any questions or need further information, don't hesitate to reach out to us. At QL Biotech, we are committed to delivering quality, innovation, and reliability — one Rota Virus Test at a time.