QL Biotech introduces its Malaria PF/PV Rapid Test, a groundbreaking tool in the detection of HIV 1&2 via a versatile and effective testing device. This advanced membrane-based immunoassay enables medical professionals and diagnostic labs to detect the presence of antibodies related to HIV 1 & 2. The test can be conducted using various sample types like whole blood, serum, or plasma, providing unprecedented convenience and effectiveness. The science behind this innovative product lies in its qualitative approach. It focuses on identifying antibodies to HIV 1&2 in the sample collected, thereby delivering direct, accurate results. The Malaria PF/PV Rapid Test actively responds to the global need for reliable, quick diagnostic solutions, particularly in the ongoing battle against HIV.

• 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.

Through continual research and development, QL Biotech has successfully created a product that meets high industry standards, promising quality and dependability. The Malaria PF/PV Rapid Test is not just another addition to our product line – it is a testament to our commitment to advancing healthcare solutions through cutting-edge biotechnology. Altogether, it is clear that the Malaria PF/PV Rapid Test, designed for the detection of HIV 1&2, offers an unparalleled level of diagnostic proficiency. It delivers accurate results efficiently, providing an essential tool for healthcare professionals in their strive to combat HIV. By opting for QL Biotech's Malaria PF/PV Rapid Test, one chooses a path of swift, reliable diagnosis, ultimately elevating patient care and health outcomes.