At QL Biotech, we take pride in our commitment to introducing innovative diagnostic solutions to ensure patient safety worldwide. To this end, we present our breakthrough Mycoplasma Pneumoniae Test, an innovative test designed for the proficient detection of HIV 1&2. Our product is a qualitative membrane-based immunoassay, capable of detecting antibodies to HIV 1 and HIV 2 effectively in whole blood, serum, or plasma. Drawing from the most advanced medical and scientific research, our test offers an unparalleled detection solution for HIV, contributing significantly to early diagnostics and timely treatments. The Mycoplasma Pneumoniae Test employs cutting-edge technology to target the HIV 1&2 antibodies in the patient's blood. The test is swift, accurate, and user-friendly, designed to provide healthcare professionals with the rapid results necessary for a swift diagnosis.

• 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.

Ensuring patient safety and enhancing the diagnostic efficiency, our reliable Mycoplasma Pneumoniae Test reduces the stress of waiting for results. It maximizes accuracy, enabling healthcare providers to promptly and effectively implement treatment strategies for each individual patient. At QL Biotech, we believe in the power of advanced diagnostic solutions. Our Mycoplasma Pneumoniae Test is a testament to our commitment to making reliable, practical, and cutting-edge diagnostic tools available to the global healthcare community. Providing accurate and quick results, the Mycoplasma Pneumoniae Test is a key player in the early detection and successful management of HIV 1&2, ensuring a healthier future for all.