[Product Name] Generic Name: Rabies Virus Antigen Rapid Test Card (Colloidal Gold Method)
[Packaging Specification] 50T/box
[Principle] This reagent is made using the principle of colloidal gold immunochromatography (GICA). After adding the sample to the sample well, it moves along the chromatographic membrane together with the colloidal gold label. If the rabies virus resistance principle is present in the sample, it binds with the colloidal gold marker and antibodies on the detection line, resulting in a purplish-red color. If the rabies virus resistance principle is absent, no color reaction occurs.
[Kit Composition]
Serial number | Name | 50 per box |
1. | Test card (including straw) | 50 units |
2. | Sample diluent | 50 copies |
[Storage and Shelf Life] Store in a cool, dry place (2-30°C), shelf life is 24 months.
[Sample Requirements] This test card is only suitable for detecting avian influenza virus in secretions from the trachea and cloaca of birds.
[Test Method]
1. Use a cotton swab to thoroughly wipe saliva from the mouth;
2. Unscrew the cap of the dropper bottle, remove the dropper head, insert a cotton swab into the bottle containing the sample buffer, and vigorously rotate the swab on the bottle wall at least 10 times, mixing the solution evenly so that the specimen dissolves as much as possible. Squeeze the cotton swab onto the bottle wall to squeeze out as much liquid as possible, discard the swab, reinstall the drip head, cover the bottle cap, and mix well;
3. Remove the test card from the sealed bag and place it on a flat surface;
4. Use a dropper bottle to hang vertically, slowly and drop by drop, add 2-3 drops to the sample well on the detection card;
5. Leave at room temperature for 10-15 minutes to determine the result; after 15 minutes, the color development is invalid.ent is invalid.
[Result Judgment]

1. Negative: In the observation hole, only a purplish-red line appears in the reference line area (C).
2. Positive: In the observation well, both the detection line area (T) and the control line area (C) show purple-red lines.
3. Ineffective: No purplish-red lines appear in the reference line area (C) inside the observation hole.
[Diagnostic Reference]
If the test result is negative, it indicates no rabies virus antigen in the sample. If corresponding acute symptoms appear, rabies virus infection cannot be ruled out; If the test result is positive, it indicates rabies virus antigen in the sample, which may indicate rabies virus infection and should be analyzed in combination with clinical and other methods.
[Limitations of the Test Method]
This test card is for screening only and does not serve as a basis for diagnosis.
[Notes]
1. Please read the manual carefully before testing. All reagents provided by this product are for use only.
2. Do not use liquids not required by [sample requirements] as negative controls.
3. Products that are expired or have damaged aluminum foil bags must not be used.
4. When removing the test card from the refrigerator, it should be opened after returning to room temperature. Once opened, the test card should be used as soon as possible to avoid deterioration after moisture.
5. Avoid contact with the chromatography film at the sample holes and detection windows on the test card.
6. Test waste should be considered pollutants and properly handled according to local regulations.