At QL Biotech, we consistently excel in providing competent solutions for accurate diagnosis and detection of various diseases. One such notable invention is our S.typhoid/S. Para typhi Ag Rapid Test Device, tailored to detect HIV 1&2 antibodies, ensuring reliable results and prompt diagnosis. The Device's superior functionality is hinged on its qualitative, membrane-based immunoassay approach. It accurately identifies the presence of antibodies to HIV 1/2 in whole blood, serum, or plasma samples. Our S.typhoid/S. Para typhi Ag Rapid Test Device goes beyond providing speedy results. With its precise technology, healthcare professionals across the globe trust it for accurate and reliable results. Not only does it speed up the diagnostic process, but it also allows for the implementation of appropriate treatment options faster. The HIV 1/2 Human Immunodeficiency Virus Rapid Test Device operates on the principle of membrane-based immunoassay. This means that the test is designed to detect antibodies that the body produces in response to the HIV 1/2 virus. The detection of these antibodies helps in the timely and accurate diagnosis of HIV 1/2.

• HIV 1/2 Rapid Test Strip(Whole Blood/Serum/Plasma)
  Allow the test strip, specimen, buffer, and/or controls to equilibrate to room temperature (15‐30°C) prior to testing. 
  1. Remove the test strip from the foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed within one hour. 
  2. Peel off the tape from the test card, and stick the test strip in the middle of test card with arrows pointing down on the test card. 
  For Serum, Plasma or Venipuncture Whole Blood specimen: Hold the dropper vertically and transfer 2 drops of serum, plasma or venipuncture whole blood (approximately 80 L) to the 
  “Specimen Pad” of the test strip, then add 1 drop of buffer (approximately 40L) and start the timer. 
  For Fingerstick Whole Blood specimen: 
  To use a capillary tube: Fill the capillary tube and transfer approximately 80L of fingerstick whole blood specimen to the “Specimen Pad” of the test strip, then add 1 drop of buffer (approximately 40L) and start the timer. 
  To use hanging drop: Allow 2 hanging drops of fingerstick whole blood specimen to fall into the center of the “Specimen Pad” on the test strip, then add 1 drop of buffer (approximately 
  40L) and start the timer. 
  3. Wait for the colored line(s) to appear. The result should be read at 15 minutes. Do not interpret results after 20 minutes.
  HIV 1/2 Rapid Test Strip（Serum/Plasma）
  HIV 1/2 Rapid Test Device (Whole Blood/Serum/Plasma)
  Allow the test device, specimen, buffer, and/or controls to equilibrate to room temperature 
  (15‐30°C) prior to testing. 
  1. 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. 
  2. Place the test device on a clean and level surface. Hold the dropper vertically and transfer 2 drops of serum, plasma (approximately 80L) to the specimen well (S) of the sample pad then add 1 drop of buffer (approximately 40L) and start thetimer. 
  3. Wait for the colored line(s) to appear. The result should be read at 10 minutes. Do not interpret results after 20 minutes. 
  HIV 1/2 Rapid Test Device（Serum/Plasma）
  Allow the test device, specimen, buffer, and/or controls to equilibrate to room temperature (15‐30°C) prior to testing. 
  1. 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. 
  2. Place the test device on a clean and level surface. 
  For Serum, Plasma specimen: Hold the dropper vertically and transfer 2 drops of serum, plasma (approximately 80L) to the specimen well (S) of the test device, then add 1 drop of buffer (approximately 40L) and start the timer. 
  3. Wait for the colored line(s) to appear. The result should be read at 10 minutes. Do not interpret results after 20 minutes.

INVALIDRESULT:

Control line (C) falls to appear. Insufficient buffer volume or incorrect procedural techniques are the most likely reasons for control line failure.

Review the procedure and repeat the procedure with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

*NOTE: The intensity of the color in the test line region (T) will vary depending on the concentration of HIV antibodies present in the specimen. Therefore, any shade of colored in the test region (T) should be considered positive.

At QL Biotech, we understand the gravity of diseases like HIV, hence, our S.typhoid/S. Para typhi Ag Rapid Test Device is designed to deliver results with high sensitivity and specificity. It stands as a testament to QL Biotech's commitment towards improved healthcare services, ensuring swift, accurate, and affordable diagnostic solutions. In a rapidly evolving healthcare sector, QL Biotech stands at the forefront with its innovative S.typhoid/S. Para typhi Ag Rapid Test Device – a reliable medical aide for an effective, quick, and accurate diagnosis of HIV 1/2. Trust in QL Biotech's exceptional technological solutions, because we strive to ensure healthcare professionals are equipped with the best diagnostic aids.