Reliable and Efficient Malaria PV/Pan Test from 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, a leading name in the biotechnology industry, is proud to present the Malaria PV/Pan Test. This innovative product stands as a testament to our commitment to quality, efficiency, and the wellbeing of individuals worldwide. The Malaria PV/Pan Test harnesses cutting-edge technology to offer rapid and accurate detection of malaria. This Malaria PV/Pan Test promises results that are not only swift but also reliable; a key factor in the management and treatment of malaria. The test is easy to use, eliminating the need for complex procedures or specialist knowledge. This makes it an ideal choice for various environments, from hospitals and laboratories to remote areas where resources may be limited. The Malaria PV/Pan Test by QL Biotech achieves the delicate balance between speed and precision. A positive result is indicated by the presence of two distinct bands in the result window of the device. Negative test results only show one band, while the absence of bands indicates that the test was invalid.

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.




QL Biotech's Malaria PV/Pan Test is a significant leap forward in combating malaria. Our novel approach reduces the likelihood of false positives and negatives, making it a versatile and dependable tool in malaria management. QL Biotech remains at the forefront of diagnostic technology, crafting solutions that empower healthcare professionals and facilitate better patient outcomes. With the Malaria PV/Pan Test, we bring you an efficient, accurate, and user-friendly diagnostic tool that redefines malaria testing. Trust QL Biotech with your testing needs and experience the difference that precision and quality can make.

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