Rabies Virus Antibody Rapid Test

• PRINCIPLE

• The Rabies Virus Antibody Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window for the observation of assay running and result reading. The testing window has an invisible T (test) zone and a C (control) zone before running the assay. When the treated sample was applied into the sample hole on the device, the liquid will laterally flow through the surface of the test strip and react with the pre-coated recombinant antigen. If the Rabies antibodies level is above 0.5IU/mL in the specimen, a visible T line will appear. The C line should always appear after a sample is applied, which indicates a valid result.

• REAGENTS AND MATERIALS

• Test devices, with disposable droppers

• Assay buffer  

• Products Manual

• STORAGE AND STABILITY

• The kit can be stored at room temperature (4-30°C). The test kit is stable through the expiration date (24 months) marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight.

• TEST PROCEDURE

• Bring all materials, including specimen and test device, recover to 15-25ºC before running the assay.

• Remove the test device from the foil pouch and place it horizontally.

• Using the disposable dropper, place 2 drops of serum or plasma into sample hole "S" of the test device. Immediately place 1drop of assay buffer into the sample hole.

• Interpret the result in 10-15 minutes. Result after 15 minutes is considered as invalid.

• INTERPRETATION OF RESULTS

• Positive (+): The presence of both "C" line and zone "T" line, no matter T line is clear or vague.

• Negative (-): Only clear C line appear. No T line.

• Invalid: No colored line appears in C zone. No matter if T line appears.

• PRECAUTIONS

• All reagents must be at room temperature before running the assay.

• Do not remove test cassette from its pouch until immediately before use.

• Do not use the test beyond its expiration date.

• The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers.

• All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states.

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