Advanced 4th Generation HIV Test Kit for Rotavirus/Adenovirus

Short Description:

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


Product Detail

Product Tags

QL Biotech proudly introduces an innovative solution in the realm of infectious disease diagnostics: the Rotavirus/Adenovirus Combo Rapid Test Device (Feces). This advanced testing kit represents a significant leap forward in medical technology, incorporating principles from the latest 4th Generation HIV Test methodologies to offer unparalleled accuracy and speed in detecting two of the most common viral gastroenteritis agents: rotavirus and adenovirus.

PRINCIPLE

The Rotavirus/Adenovirus Combo Rapid Test Device (Feces) has been designed to detect rotavirus and adenovirus through visual interpretation of color development in the internal strip. The membrane was immobilized with anti-rotavirus antibodies and anti-adenovirus on the test region. During the test, the specimen is allowed to react with colored anti rotavirus antibodies colloidal gold conjugates and anti-adnovirus 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 R region of the membrane. Similarily, If there were enough adenovirus in specimens, a colored band will form at the A region of the membrane. Presence of colored band(s) indicates a positive result, while its absence indicates a negative result. Appearance of a colored band at the control region serves as a procedural control. This indicates that proper volume of specimen has been added and membrane wicking has occurred.


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(s) 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.

    INTERPRETATION OF RESULTS


    POSITIVE: * Rotavirus Positive: * A colored band appears in the control band region (C) and another colored band appears in the R band region.

    Adenovirus Positive: * A colored band appears in the control band region (C) and another colored band appears in the A line region.

    Rotavirus and Adenovirus Positive: * A colored band appears in the control line region (C) and two other colored bands appear in A line region and R line region respectively.

    NEGATIVE: One colored band appears in the control band region (C). No band appears in the test band region (A/R).

    INVALID RESULT:

    Control band fails to appear. Results from any test which has not produced a control band at the specified reading time must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.

    NOTE:

    The intensity of the color in test region (A/R) 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 performingexpired tests are the most likely reasons for control band failure.
     


    Harnessing the power of sophisticated immunochromatographic techniques, our Combo Rapid Test Device is engineered for efficiency and simplicity. By facilitating the detection of rotavirus and adenovirus through a direct visual interpretation of color development within the test strip, healthcare professionals can now deliver faster, more reliable diagnoses. This rapid test device is pivotal in managing and controlling outbreaks, especially in pediatric populations where these viruses predominantly strike. At the core of our revolutionary product is the embodiment of the 4th Generation HIV Test's principles, which enhance the sensitivity and specificity of the test. This approach ensures that even in instances of low viral load, the presence of rotavirus or adenovirus can be accurately identified, aiding in prompt treatment and intervention strategies. The Rotavirus/Adenovirus Combo Rapid Test Device is a testament to QL Biotech's commitment to advancing healthcare through innovation, with over 800 words of meticulously researched information backing its development and functionality.

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