Tuberculosis Rapid Test Kit: Swift, Precise Analysis by QL Biotech

Short Description:

The H. Pylori Ab Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies to H. Pylori in serum or plasma to aid in the diagnosis of H.


Product Detail

Product Tags

QL Biotech proudly introduces the Tuberculosis Rapid Test Kit, a breakthrough product designed for swift and accurate detection of Tuberculosis. Our test kit is built on advanced scientific principles and innovative technology, promising high accuracy and reliable results. Tuberculosis, a deadly disease caused by Mycobacterium tuberculosis, poses a significant threat worldwide. Early and accurate diagnosis is critical to prevent its spread and ensure effective treatment. Recognising this need, QL Biotech has developed the Tuberculosis Rapid Test Kit, a product designed to simplify detection and bring lab-level accuracy to your fingertips. The principle behind our product is to detect the presence of tuberculosis antigens in the patient's sample. This rapid test strip/device utilises anti-tuberculosis antibodies conjugated to particles, capable of precise and swift detection. When a sample is applied to the test device, it reacts with the antibodies, and if the tuberculosis antigen is present, it forms a visible line, indicating a positive result. The presence of two lines on the test device signifies a positive result, while one line suggests a negative result. This innovative Tuberculosis Rapid Test Kit does not require any specialized equipment or professional skills, making it an ideal choice for initial screening and point-of-care testing in diverse settings. With simple steps, you can obtain dependable results within minutes.

PRINCIPLE

The H. Pylori Ab Rapid Test Strip (Serum/ Plasma) is a qualitative membrane strip based immunoassay for the detection of H. Pylori antibodies in whole blood, serum or plasma. In this test procedure, the test strip is immersed in the specimen or specimen containing buffering solution. This specimen migrates chromatographically along the length of the test strip and interacts with the reagents contained on the test strip. If the specimen contains H. Pylori antibodies, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain H.

Pylori antibodies, a colored line will not appear in this region indicating a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.


Product Detail

Brand: QL

Specimens: : Serum/Plasma

Reading time:20 minutes.

Pack:25 T

STORAGE: 2‐30°C

KIT COMPONENTS(Device)

Individually packed test devices/strips 

Disposable pipettes

Buffer

Package insert

 

Brand: QL

Specimens: : Whole Blood/Serum/Plasma

Reading time:20 minutes.

Pack:25 T

STORAGE: 2‐30°C

Individually packed test devices/strips 

Disposable pipettes

Buffer

Package insert

PROCEDURE

  • Allow the test device, specimen, buffer, and/or controls to equilibrate to room temperature (15-30°C) prior to testing.
  • Remove the test device from the foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed within one hour.
  • Place the test device on a clean and level surface.
  • Hold the dropper vertically and transfer 2 drops of sample to the specimen well (S) of the test device, then add 1 drop of buffer and start the timer.
  • Wait for the red line(s) to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.

INTERPRETATION OF RESULTS


  • POSITIVE RESULT:

    * A colored band appears in the control band region (C) and another colored band appears in the T band region. 
    NEGATIVE RESULT: 
    One colored band appears in the control band region (C). No band appears in the test band region (T). 
    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: 
    1. 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. 
    2. Insufficient specimen volume, incorrect operation procedure, or performing expired tests are the most likely reasons for control band failure.




While focusing on user convenience and simplicity, QL Biotech does not compromise on quality and accuracy. Our Tuberculosis Rapid Test Kit is compliance assured and guarantees precise results, contributing significantly to the global fight against tuberculosis. QL Biotech remains committed to delivering innovative diagnostics solutions. Our Tuberculosis Rapid Test Kit represents our pledge to establishing healthier communities worldwide. Trust in QL Biotech, your reliable partner in accurate, swift Tuberculosis detection.

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