Innovative HEV IgG/IgM Test Cassette by QL Biotech: Quick, Accurate H.Pylori Ab Detection

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

As a key player in the biotech industry, QL Biotech is delighted to bring you our state-of-the-art HEV IgG/IgM Test Cassette, an essential tool for the rapid and accurate detection of H.Pylori Ab. Our H.Pylori Ab Rapid Test Strip/Device takes advantage of the latest advancements in bioscience, ensuring a hassle-free diagnosis of Hepatitis E Virus (HEV) through IgG and IgM antibodies. Our HEV IgG/IgM Test Cassette is designed with your convenience in mind, allowing swift testing and instant results. It provides high sensitivity and specificity, enabling healthcare professionals to efficiently detect the presence or absence of H.Pylori Ab in test samples. QL Biotech is at the forefront of providing cutting-edge diagnostic tools, and our HEV IgG/IgM Test Cassette is a testament to our commitment to excellence. This particular product stands in line with our commitment to meet and surpass the needs of healthcare practitioners globally.

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.




Our HEV IgG/IgM Test Cassette delivers a rapid, accurate, and hassle-free solution for H.Pylori Ab detection. We are committed to staying at the forefront of biotech advancements, ensuring that our products align with the demands of a fast-paced healthcare environment. With the HEV IgG/IgM Test Cassette, we aim to provide an effective solution for diagnosing Hepatitis E Virus, contributing to improved patient outcomes worldwide. The versatility of the HEV IgG/IgM Test Cassette sets it apart from other testing strips/devices. This product by QL Biotech promises unparalleled efficiency and accuracy, making it a trusted choice for healthcare professionals around the world. Take a step towards advanced diagnostics with the HEV IgG/IgM Test Cassette by QL Biotech. Experience accuracy, dependability, and speed like never before. Choose QL Biotech products and join us in our journey of revolutionising the world of diagnostics.

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