In the domain of medical diagnostics, QL Biotech emerges as a leader with its innovative solutions tailored to meet the pressing needs of rapid and reliable disease detection. Among its flagship products stands the Malaria PF/PV Rapid Test Kit – a cornerstone in the fight against one of the most prevalent and dangerous diseases worldwide. This test kit is designed to offer clinical professionals and health practitioners an efficient means of diagnosing Malaria, providing results that are both quick and accurate, thereby enabling timely treatment and management of the disease.

• 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.

The Malaria PF/PV Rapid Test Device is a thoughtfully engineered diagnostic tool that utilizes a highly specific and sensitive membrane-based immunoassay. This test is capable of detecting all four types of Malaria parasites (P. falciparum, P. vivax, P. ovale, and P. malariae) in human blood through the identification of Plasmodium-specific antigens. The procedure requires just a simple step of placing a drop of the patient’s blood onto the test strip or device, followed by the addition of the buffer. Within 15 to 20 minutes, the presence of a colored line indicates a positive result for Malaria, while its absence signifies a negative outcome. The test's high degree of specificity and sensitivity ensures that healthcare providers can trust the results, facilitating prompt and appropriate treatment decisions. QL Biotech's Malaria PF/PV Rapid Test Kits embody the company’s commitment to enhancing public health through the provision of reliable, accessible, and easy-to-use diagnostic tools. By simplifying the process of Malaria detection without compromising on accuracy, these kits play a pivotal role in the global effort to control and eventually eradicate this life-threatening disease. The test's design prioritizes both healthcare practitioners' and patients' needs, ensuring that the fight against Malaria is bolstered by technology that is not only advanced but also user-friendly and widely accessible. With QL Biotech's Malaria PF/PV Rapid Test Kits, medical professionals have a powerful tool in their arsenal for the early detection and treatment of Malaria, paving the way for better outcomes and a healthier future.