
Babesia Ab
- Discription: Canine Babesia Antibody 1.0 Rapid Test (Babesia Ab)
- Catalog No.: JCA033D
- Principle: Sandwich lateral flow immunochromatographic assay
- Specification: 10 tests/kit
- Assay Time: 5-10 minutes
- Shelf life: 24months
Stable, Reliable, Affordable
Description
Canine Babesia Antibody 1.0 Rapid Test (Babesia gibsoni Ab)
Catalog No.: JCA033D
¤ INTENDED USE
The Canine Babesia Antibody 1.0 Rapid Test is a test cassette to diagnose the presence of Babesia gibsoni antibodies (Babesia Ab) in dog’s serum or plasma specimen.
Assay Time: 5-10 minutes
Specimen: Serum, plasma or Whole blood.
¤ PRINCIPLE
The Babesia Ab Test is based on sandwich lateral flow immunochromatographic assay.
¤ REAGENTS AND MATERIALS
- Test devices, with disposable droppers
- Assay buffer
- Cotton swabs
- 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
- Allow all materials, including specimen and test device, recover to 15-25℃ before running the assay.
- Take out the test device from the foil pouch and place it horizontally.
- Using the capillary dropper to place 1 drop (approx. 10μL) of the prepared specimen into the sample hole “S” of the test device. Then drop 3 drops (approx. 80μL) of the assay buffer into the sample hole immediately.
- Interpret the result in 5-10 minutes. Result after 10 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.
¤ LIMITATION
The Babesia Antibody 1.0 Rapid Test(Babesia Ab) is for in vitro veterinary diagnosis use only. The test could not distinguish different Babesia species. Some Babesia canis may be reacting with the Babesia gibsoni test. All result should be considered with other clinical information available with veterinarian. It is suggested to apply a further confirmative method such as RT-PCR when positive result was observed.
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J&G Biotech Ltd (Reg. No.: 08419172)
326 Cleveland Road, London, England E18 2AN, UK

