Fast & Accurate Syphilis Test Cassette by QL Biotech

Short Description:

The Typhoid Ag Rapid Test Device (Feces) is a lateral flow immunoassay for the simultaneous detection and differentiation of Salmonella Typhoid in feces.


Product Detail

Product Tags

In the world of rapid medical diagnostics, the need for accurate, reliable, and convenient testing solutions is paramount. QL biotech proudly introduces its latest innovation in health diagnostics: the Typhoid Ag Rapid Test Device, now re-engineered to meet the demanding accuracy of syphilis detection - the Accurate Syphilis Test Cassette. Drawing upon our extensive expertise in biotechnological research and development, we have created a product that not only surpasses industry standards for typhoid testing but also sets a new benchmark for syphilis detection.

PRINCIPLE

The Typhoid Ag Rapid Test Device (Feces) is a lateral flow chromatographic immunoassay. The test cassette consists of: 1) a burgundy colored conjugate pad containing S. typhoid antibody conjugated with colloid gold, 2) a nitrocellulose membrane strip containing two test bands (S.typhoid bands) and a control band (C band). The S. typhoid band is pre-coated with monoclonal anti- S. typhoid for the detection of S. typhoid Ag, and the C band is pre-coated with goat anti mouse IgG. When an adequate volume of test specimen is dispensed into the sample well of the cassette, the test specimen migrates by capillary action across the test cassette. S. typhoid Ag if present in the patient specimen will bind to the S. typhoid Ab conjugates. The immunocomplex is then captured on the membrane by the pre-coated S. typhoid antibody, forming a burgundy colored S. typhoid band, indicating a S. typhoid positive test result. Absence of any test bands 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 Mouse IgG/Mouse IgG-gold conjugate regardless of the color development on any of the test bands. Otherwise, the test result is invalid and the specimen must be retested with another device.


Product Detail

            • Brand: QL

              Specimens: : Faces

              Reading time:10 minutes.

              Pack:20 T

              STORAGE: 2‐30°C

              KIT COMPONENTS

              • Test devices
              • Droppers
              • Single Buffer
              • Package insert

 

  • ASSAY PROCEDURE

        • Bring tests, specimens, buffer and/or controls to room temperature (15-30°C) before use.

          1. Specimen collection and pre-treatment: 
          1) Unscrew and remove the dilution tube applicator. Be careful not to spill or spatter solution from the tube. Collect specimens by inserting the applicator stick into at least 3 different sites of the feces. 
          2) Place the applicator back into the tube and screw the cap tightly. Be careful not to break the tip of the dilution tube. 
          3) Shake the specimen collection tube vigorously to mix the specimen and the extraction buffer. Specimens prepared in the specimen collection tube may be stored for 6 months at -20°C if not tested within 1 hour after preparation. 
          2. Testing 
          1) Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. To obtain a best result, the assay should be performed within one hour. 
          2) Using a piece of tissue paper, remove the tip of the dilution tube. Hold the tube vertically and dispense 3 drops of solution into the specimen well (S) of the test device. 
          Avoid trapping air bubbles in the specimen well (S), and do not drop any solution in observation window. 
          As the test begins to work, you will see color move across the membrane. 
          3. Wait for the colored band(s) to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.


        INTERPRETATION OF ASSAY RESULT

        • 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.
          •  


        The evolution from our Typhoid Ag Rapid Test Device to the Accurate Syphilis Test Cassette has been driven by a commitment to providing healthcare professionals and patients with a tool that is not just rapid but is also imbued with a level of accuracy that instills confidence in every result. This lateral flow chromatographic immunoassay represents the pinnacle of our scientific achievements. Utilizing a meticulously designed antigen-antibody reaction, the Accurate Syphilis Test Cassette offers an unparalleled sensitivity and specificity in syphilis testing. This ensures that both healthcare providers and patients can trust in the results, leading to timely and appropriate medical interventions. Our commitment to excellence extends beyond the technical aspects of the Accurate Syphilis Test Cassette. Recognizing the importance of user experience, we have crafted this device to be as intuitive and user-friendly as possible. Whether it is a medical professional conducting multiple tests in a clinical setting or an individual seeking personal health assurance, the Accurate Syphilis Test Cassette guarantees a straightforward testing process. From the moment you open the package, you will find everything needed for a complete test, including clear instructions that guide you through every step. The design is not just about ease of use but also ensures the integrity of the sample and the accuracy of the test results. With the Accurate Syphilis Test Cassette, QL biotech is not just presenting a product but a comprehensive solution for syphilis detection that sets new standards in rapid testing technology.

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