Detection of Canine Lyme Antibody with the QL Biotech Ferritin Rapid Test Device
PRINCIPLE
The Human Ferritin Rapid Test Device (Whole blood/Serum/Plasma) is a qualitative, lateral flow immunoassay for the detection of human Ferritin in human whole blood, serum and plasma. The membrane is pre‐coated with anti‐ferritin antibody on the test line region of the strip. During testing, the specimen reacts with the particle coated with anti‐ferritin antibody. The mixture
migrates upward on the membrane chromatographically by capillary action to react with anti‐ferritin antibody on the membrane and generate a colored line. The presence of this colored
line in the test region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear in the control line region
indicating that the proper volume of specimen has been added and membrane wicking has occurred.
PRECAUTIONS
For professional in vitro diagnostic use only. Do not use after expiration date.
- ● The test device should remain in the sealed pouch until use.
- ● Do not eat, drink or smoke in the area where the specimens or kits are handled.
- ● Do not use if pouch is damaged.
- ● Handle all specimens as if they contain infectious agents. Observe established precautionsagainst microbiological hazards throughout the procedure and follow the standard proceduresfor proper disposal of specimens.
- ● Wear protective clothing such as laboratory coats, disposable gloves or eye protection whenspecimens are being tested.
- ● Humidity and temperature can adversely affect results.
DIRECTIONS FOR USE
Allow test device, specimen, buffer and/or controls to reach room temperature (15‐30°C) 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.
For Whole Blood, Serum or Plasma specimens:
Hold the dropper vertically and transfer 2 drops of specimen (or approximately 50 µL) to the specimen well (S) of the test device, then add 1 drop of buffer and start the timer.
For Fingerstick Whole Blood specimens:
To use a capillary tube: Fill the capillary tube and transfer approximately 50 µL (or 2 drops) of fingerstick whole blood specimen to the specimen well (S) of the test device, then add 1 drop of buffer and start the timer.
3. Wait for the colored line(s) to appear. Read results at 10 minutes. Do not interpret results after 20 minutes.
PERFORMANCE CHARACTERISTICS
Accuracy
The Transferrin Rapid Test Device (Feces) has been compared with another leading commercial rapid test using clinical specimens.
|
Method |
Other Rapid Test |
Total Results |
||
|
TF Rapid Test Device
|
Results |
Positive |
Negative |
|
|
Positive |
20 |
0 |
20 |
|
|
Negative |
0 |
20 |
20 |
|
|
Total Results |
20 |
20 |
20 |
|
Relative Sensitivity: >99.9 %
Relative Specificity: >99.9 %
Relative Accuracy: >99.9 %
Sensitivity
The Human Ferritin Rapid Test Device (Whole blood/Serum/Plasma) can detect the levels of human ferritin as low as 20 ng/mL ferritin.
Interfering Substances
The Human Ferritin Rapid Test Device (Whole blood/Serum/Plasma) has been tested and no interference was observed in specimens containing 110mg/mL human albumin, 6 mg/mL bilirubin, 5 mg/mL cholesterol and 15 mg/mL triglycerides.
Every detection process undergoes rigorous quality checks to guarantee the accuracy of the Detection of Canine Lyme Antibody. As a leader in the market, QL Biotech constantly innovates to ensure the best quality products for its customers. Our Ferritin Rapid Test Device offers you a seamless experience in the Detection of Canine Lyme Antibody, whether you are a healthcare provider or an individual. With QL Biotech, you can be assured of fast, reliable, and efficient detection methods, designed to facilitate diagnosis and enhance patient care. Try the QL Biotech Ferritin Rapid Test Device today for unparalleled accuracy in the Detection of Canine Lyme Antibody.