QL Biotech proudly presents the innovative One Step TOXO IgG/IgM Test, reengineered and optimized for the rapid detection of syphilis infections. This cornerstone product, now enhanced for even quicker and more dependable diagnoses, embodies our commitment to advancing medical diagnostics. Our state-of-the-art Quick Read Syphilis Test Kit is the epitome of diagnostic efficiency and reliability, designed to meet the urgent needs of healthcare providers and patients alike.

• PRINCIPLE

  • It is a qualitative membrane strip based immunoassay for the detection of TOXO antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing TOXO recombinant envelope antigens conjugated with Colloid gold (TOXO conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-TOXO, T2 band is coated with antibody for the detection of IgG anti-TOXO, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-TOXO, if present in the specimen, will bind to the TOXO conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a TOXO IgG positive test result and suggesting a recent or repeat infection. IgM anti-TOXO if present in the specimen will bind to the TOXO conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a TOXO IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device.

  
  

  TEST PROCEDURE

  Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing. 
  1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible. 
  2. Place the test device on a clean and level surface. 
  3. Hold the dropper vertically and transfer 1 drop of specimen (approximately 10μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below. 
  4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes. 
  Notes: 
  Applying sufficient amount of specimen is essential for a valid test result. If migration (the wetting of membrane) is not observed in the test window after one minute, add one more drop of buffer to the specimen well.
•  

IgM Positive:* The colored line in the control line region (C) appears and a colored line appears in test line region 1 (T1). The result is positive for Toxo virus specific-IgM antibodies and is indicative of primary Toxo infection.

IgG Positive:* The colored line in the control line region (C) appears and a colored line appears in test line region 2 (T2). The result is positive for Toxo virus specific-IgG and is probably indicative of secondary Toxo infection.

IgG and IgM Positive:* The colored line in the control line region (C) appears and two colored lines should appear in test line regions 1 and 2 (T1 and T2). The color intensities of the lines do not have to match.

The result is positive for IgG & IgM antibodies and is indicative of secondary Toxo infection.

The colored line in the control line region (C) appears. No line appears in test line regions 1 or 2 (T1 or T2).

INVALID RESULT:

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 devic 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 cannot 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.

 

At the heart of our Quick Read Syphilis Test Kit lies a revolutionary testing mechanism driven by the cutting-edge lateral flow chromatographic immunoassay technology. Utilizing the double antigen-sandwich method, this advanced diagnostic tool offers unparalleled accuracy and speed. The principle underlying our test kit ensures that both IgG and IgM antibodies are detected with high sensitivity and specificity, providing a comprehensive insight into the infection status of the patient. With QL Biotech's Quick Read Syphilis Test Kit, healthcare professionals can now benefit from a streamlined testing process. The robust design of our test kit allows for the rapid identification of syphilis antibodies, delivering results in mere minutes. This not only facilitates early and accurate diagnosis but also significantly enhances the effectiveness of subsequent treatment and intervention strategies. By integrating our Quick Read Syphilis Test Kit into your diagnostic repertoire, you can assure your patients of a quick, reliable path towards recovery, embodying QL Biotech's mission to innovate for healthier lives.