Haematology analysers
Blood Gas and Electrolyte Analyzers
Rapid test for detection of syphilis (Syphilis)
A highly sensitive in vitro immunochromatographic rapid test designed for the qualitative detection of antibodies to Treponema pallidum (the causative agent of syphilis) in human whole blood, serum, or plasma samples.
Ease of use, rapid results (within 10–15 minutes), and no need for specialized laboratory equipment make this test kit an effective tool for initial syphilis screening in clinics, laboratories, infection prevention centers, and field settings.
The test ensures high accuracy due to its specific detection of syphilis antibodies. A reactive result requires confirmation using treponemal laboratory tests (e.g., TPHA or FTA-Abs).
TEST KIT CONTENTS
Test Kit Contents
Test cassette
Pipette
Buffer solution
Instructions for use
TEST PROCEDURE
Before testing, bring the test cassette, buffer, and sample to room temperature (15–30°C).
1. Remove the test cassette from the sealed pouch and use it as soon as possible. For best results, testing should be performed within one hour.
2. Place the test cassette on a clean, level surface. Label the test with sample identification.
For venous whole blood samples:
Hold the dropper vertically and transfer 2 drops of whole blood (approximately 50 µL) into the sample well (S) of the test cassette, then add 1 drop of buffer (approximately 40 µL) and start the timer.For fingerstick whole blood samples:
Apply 2 drops of fingerstick whole blood into the sample well (S) of the test cassette, then add 1 drop of buffer (approximately 40 µL) and start the timer.For serum or plasma samples:
Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 75 µL) into the sample well (S) of the test cassette and start the timer. Avoid air bubbles in the sample well (S), and do not add any solution to the result area.
3. Wait for the colored line to appear. Read results at 10 minutes.
INTERPRETATION OF RESULTS
POSITIVE
Two colored lines appear on the membrane: one in the control region (C), and one in the test region (T).
A positive result indicates that the sIgE concentration exceeds the detectable level.
NEGATIVE
Only one colored line appears in the control region (C). No line appears in the test region (T). A negative result indicates that the sIgE concentration is below the defined level.
