Dengue Igg/Igm Rapid Test - Rotavirus Detection Device by QL Biotech

Short Description:

The Rotavirus Rapid Test Device (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of rotavirus in human fecal specimens. This kit is intended to be used as an aid in the diagnosis of rotavirus infection. 


Product Detail

Product Tags

QL Biotech brings to you our latest innovation - the Dengue Igg/Igm Rapid Test, a cutting-edge device designed specifically for the rapid detection of rotavirus in fecal samples. This state-of-the-art detection tool offers remarkable accuracy and delivers fast, reliable results, making it a game-changer in the field of medical diagnostics. The Dengue Igg/Igm Rapid Test Device stands out by relying on the principle of colorimetric determination. This mechanism is based on the visual interpretation of color changes within an internal strip. When the test is conducted, a reaction occurs causing the strip to change color. The shift in color is an indicator of the presence or absence of rotavirus, thus providing a timely and efficient diagnosis. Our device takes a complex process and simplifies it, all while maintaining precise and reliable results. This balance of simplicity and accuracy is what sets the Dengue Igg/Igm Rapid Test Device apart in the market. Not only does the device provide rapid results, but it also brings an unparalleled level of convenience to medical professionals, enabling them to administer the test with ease and interpret the results without difficulty.

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)



    Individually packed test devices
    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 addition to its superior functionality, the Dengue Igg/Igm Rapid Test Device is also designed with user safety in mind. It complies with all necessary safety standards, ensuring that it is not only effective but also secure to use. In conclusion, the Dengue Igg/Igm Rapid Test device from QL Biotech is a revolutionary addition to the world of medical diagnostics. With its speedy results, ease of use, and high degree of accuracy, it is the optimal choice for rotavirus detection. Trust QL Biotech to deliver quality, innovation, and reliability in every product. Embrace the future of diagnostics with the Dengue Igg/Igm Rapid Test Device.

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